| NCT#: | NCT06748222 |
| NCT QR Code | ![]() |
| Title: | Harnessing E-Mindfulness Approaches for Living After Breast Cancer (HEAL-ABC) |
| Protocol: | NRG-CC015 |
| Cancer Type: | non-metastatic breast cancer which is Stage 0, I, II, or III |
| Study Sponsor: | National Cancer Institute (NCI) |
| Brief Summary: | NRG-CC015 is a prospective, randomized phase III clinical trial to evaluate the efficacy of two distinct digital approaches for delivering a mindfulness-based intervention: a live, instructor-led version delivered over Zoom (MAPs LO), and an app-based, self-paced version (MAPs App). Participants will include younger breast cancer survivors (BCS) who were diagnosed with breast cancer at or before age 50 years, have completed their primary cancer treatment (i.e., surgery, radiation, and/or chemotherapy) at least 6 months earlier, and report elevated depressive symptoms. |
| Study Type: | Interventional |
| Date Opened at SVMHS: | June 30, 2025 |
| Recruitment Status: | Recruiting |
| Study Population: | 18 Years to 50 Years (Adult ) |
| Eligibility Criteria: | The participant or a legally authorized representative must provide study-specific informed consent prior to pre-entry and, for participants treated in the U.S., authorization permitting release of personal health information. The participant must have been greater than or equal to 18 or less than or equal to 50 years of age at the time of breast cancer diagnosis. The participant must have a first-time diagnosis of non-metastatic breast cancer which is Stage 0, I, II, or III. The participant must have a score of greater than or equal to 5 and less than or equal to 14 on the Patient Health Questionnaire-8 item (PHQ-8). Participants must have completed all primary breast cancer treatments at least 6 months prior to and no more than 5 years prior to registration. Note: Primary treatments include surgery, radiation therapy, adjuvant chemotherapy, targeted therapies (e.g., PARP (poly-ADP ribose polymerase) inhibitors, CDK4/6 inhibitors, TDM-1, pertuzumab, or immunotherapy). (Participants may still be taking adjuvant therapy with trastuzumab or adjuvant endocrine therapy or completing minor reconstructive surgery.) Participant must be able to understand, speak, read, and write in English or Spanish. Participant must be willing to participate in a 6-week program to receive training in mindfulness. Participant must be able to use a smartphone, tablet, or other digital device. Sex assigned at birth must be female. |
| Principal Investigator: | Hong Zhao, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Memorial Healthcare System & Salinas Valley Medical Clinics & Salinas Valley Memorial Hospital |
| SVMHS Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, tnielsen2@svmh.com |
| Link to ClinicalTrials.gov: | https://clinicaltrials.gov/study/NCT06748222?cond=HEAL-ABC&rank=2#study-overview |
| SCHEMA: | Schema |
National Cancer Institute “Cancer Moonshot Biobank”
| NCT#: | NCT04314401 |
| NCT QR Code | ![]() |
| Title: | National Cancer Institute “Cancer Moonshot Biobank” |
| Protocol: | Moonshot |
| Cancer Type: | Multiple cancer types: Colorectal cancer: Stage IV; Non-small cell or small cell lung cancer: Stage III/IV; Prostate cancer: metastatic prostate cancer; Gastric cancer, NOS: Stage IV; Esophageal cancer, NOS: Stage IV; Adenocarcinoma of gastroesophageal junction: Stage IV; High Grade Serous ovarian cancer: Stage III/IV; Invasive breast carcinoma: Stage III/IV; Melanoma: Stage III/IV; Acute myeloid leukemia; Multiple myeloma. |
| Study Sponsor: | National Cancer Institute (NCI) |
| Brief Summary: | This trial collects multiple tissue and blood samples, along with medical information, from cancer patients. The “Cancer Moonshot Biobank” is a longitudinal study. This means it collects and stores samples and information over time, throughout the course of a patient’s cancer treatment. By looking at samples and information collected from the same people over time, researchers hope to better understand how cancer changes over time and over the course of medical treatments. |
| Study Type: | Observational |
| Date Opened at SVMHS: | January 24, 2025 |
| Recruitment Status: | Recruiting |
| Study Population: | 13 Years and older (Child, Adult, Older Adult) |
| Eligibility Criteria: | Diagnosed with one of the following: Colorectal cancer: stage IV, Non-small cell or small cell lung cancer: stage III/IV, Prostate cancer: metastatic prostate cancer, Gastric cancer, not otherwise specified (NOS): stage IV, Esophageal cancer, NOS: stage IV, Adenocarcinoma of gastroesophageal junction: stage IV, High grade serous ovarian cancer: stage III/IV, Invasive breast carcinoma: stage III/IV, Melanoma: stage III/IV, Acute myeloid leukemia, Multiple myeloma |
| Principal Investigator: | Geetha N. Varma, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Memorial Healthcare System & Salinas Valley Medical Clinics & Salinas Valley Memorial Hospital |
| SVMHS Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, tnielsen2@svmh.com |
| Link to ClinicalTrials.gov: | https://clinicaltrials.gov/study/NCT04314401?cond=moonshot&rank=1#study-overview |
A Phase 1/2 Multiple Expansion Cohort Trial of the SOS1 Inhibitor MRTX0902 in Patients with Advanced Solid Tumors Harboring Mutations in the KRAS-MAPK Pathway
| NCT#: & Link | NCT05578092 |
| NCT QR Code | ![]() |
| Available as of: | October 14, 2024 |
| Contract: | Optimal |
| Indication Category: | Solid Tumors, NSCLC |
| Study Sponsor: | Mirati Therapeutics |
| Protocol #: | 0902-001 |
| Title: | A Phase 1/2 Multiple Expansion Cohort Trial of the SOS1 Inhibitor MRTX0902 in Patients with Advanced Solid Tumors Harboring Mutations in the KRAS-MAPK Pathway |
| Highlight Details: | NSCLC previously treated with KRAS G12C inhibitor Solid Tumor not previously treated with KRAS G12C inhibitor This is a Phase 1/2, open-label, multicenter, study evaluating the safety, tolerability, PK, PD, and anti-tumor activity of MRTX0902 alone and in combination with MRTX849 (adagrasib) in patients with advanced solid tumor malignancy harboring mutations in the KRAS-MAPK pathways. |
| Biomarkers: | KRAS G12C |
| Indication: | NSCLC, Other Solid Tumors |
| Phase: | 1/2 |
| Treatment Line: | |
| Study Drug/Test Compound: | MRTX0902 + Adagrasib |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG462 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors – Lung
| NCT#: & Link | NCT05732831 |
| NCT QR Code | ![]() |
| Available as of: | October 1, 2024 |
| Contract: | Optimal |
| Indication Category: | Solid Tumors |
| Study Sponsor: | Tango Therapeutics |
| Protocol #: | TNG462-C101 |
| Title: | A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG462 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors |
| Highlight Details: | • ECOG 0-1 • Participants with locally advanced or metastatic NSCLC (squamous or non-squamous) who meet the following criteria: • a. Progressive disease after prior treatment or after following local treatment guidelines (eg, ESMO guidelines) for the standard of care (SOC) if more strict. • b. Tested for known treatable driver mutations/alterations (eg, EGFR, ALK, and ROS1) and received at least 1 SOC targeted therapy(ies) for the known alteration, if present or after failing local treatment guidelines (eg, ESMO or study guidelines) for the SOC if more strict. • Measurable disease based on RECIST v1.1 • Documented homozygous deletion of MTAP in a tumor detected by a validated NGS test, or absence of MTAP protein in a tumor detected by a validated IHC test. • Adequate organ and hematological functions • At least 1 of the following criteria for standard-of-care therapy(ies): • a. Progression or an inadequate response to an approved SOC therapy; there is no limit to the number of prior lines of therapy • b. No approved SOC therapy • c. Patient intolerant to the available SOC therapy(ies) • d. Investigator has determined that treatment with the SOC therapy is not appropriate |
| Biomarkers: | MTAP-deletion |
| Indication: | NSCLC with MTAP deletion |
| Phase: | 2 |
| Treatment Line: | 2nd+ line |
| Study Drug/Test Compound: | TNG462 is a potent and selective oral small molecule inhibitor of PRMT5. TNG462 binds PRMT5 cooperatively with MTA to inhibit function. As an MTA cooperative inhibitor with selectivity for patients whose tumors are MTAP deleted, TNG462 addresses the 2 challenges of tumor selectivity and patient selection |
| Notes | 462 more selective/potent at a lower dose then 908 462 not brain penetrant, less risk for cognitive disturbance (but not useful for brain lesions) Phase 2 IP: TNG462 QD starting dose of 200mg PO |
| Recruitment Status: | Just In Time – ON HOLD |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
A Study of Repotrectinib in Pediatric and Young Adult Subjects Harboring ALK, ROS1, OR NTRK1-3 Alterations
| NCT#: & Link | NCT04094610 |
| NCT QR Code | ![]() |
| Available as of: | September 3, 2024 |
| Contract: | Caris |
| Indication Category: | Solid Tumors |
| Study Sponsor: | Turning Point Therapeutics, Inc |
| Protocol #: | TPX-0005-07 |
| Title: | A Study of Repotrectinib in Pediatric and Young Adult Subjects Harboring ALK, ROS1, OR NTRK1-3 Alterations |
| Highlight Details: | A Phase 1/2, Open-Label, Safety, Tolerability, Pharmacokinetics, and Anti-Tumor Activity Study of Repotrectinib in Pediatric and Young Adult Subjects With Advanced or Metastatic Malignancies Harboring ALK, ROS1, NTRK1-3 Alterations |
| Biomarkers: | NTRK FUSIONS |
| Indication: | Solid Tumors |
| Phase: | 2 |
| Treatment Line: | |
| Study Drug/Test Compound: | TPX-0005/Repotrectinib |
| Notes | Phase 1 will evaluate the safety and tolerability at different dose levels of repotrectinib in pediatric and young adult subjects with advanced or metastatic malignancies harboring anaplastic lymphoma kinase (ALK), receptor tyrosine kinase encoded by the gene ROS1 (ROS1), or neurotrophic receptor kinase genes encoding TRK kinase family (NTRK1-3) alterations to estimate the Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD) and select the Pediatric Recommended Phase 2 Dose (RP2D). Phase 2 will determine the anti-tumor activity of repotrectinib in pediatric and young adult subjects with advanced or metastatic malignancies harboring ROS1 or NTRK1-3 alterations. |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
The Caris Biorepository Research Protocol
| NCT#: & Link | NCT01499394 |
| NCT QR Code | ![]() |
| Available as of: | September 3, 2024 |
| Contract: | Caris |
| Indication Category: | Solid Tumors |
| Study Sponsor: | Caris Life Sciences |
| Protocol #: | TCBIO-001-0710 |
| Title: | The Caris Biorepository Research Protocol |
| Highlight Details: | The Biorepository for Caris Life Sciences is designed for the purpose of making quality biospecimens and associated clinical data available for research studies related to advancing precision medicine and improving care for patients. The Caris Biorepository is a repository of prospectively collected biological specimens and associated clinical and demographic data gathered from multiple sources to be stored, used and shared for research. Caris Life Sciences will maintain the data and specimens and will control access to and use of the information and specimens by multiple individuals for multiple purposes which may evolve over time. |
| Biomarkers: | |
| Indication: | Solid Tumors |
| Phase: | |
| Treatment Line: | |
| Study Drug/Test Compound: | |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
Phase 1/2 Study of MRTX849 in Patients With Cancer Having a KRAS G12C Mutation KRYSTAL-1
| NCT#: & Link | NCT03785249 |
| NCT QR Code | ![]() |
| Available as of: | July 15 2024 |
| Contract: | Caris |
| Indication Category: | Solid Tumors |
| Study Sponsor: | Mirati Therapeutics |
| Protocol #: | 849-001 |
| Title: | Phase 1/2 Study of MRTX849 in Patients With Cancer Having a KRAS G12C Mutation KRYSTAL-1 |
| Highlight Details: | ***REFERRAL ONLY*** A Phase 1/2 Multiple Expansion Cohort Trial of MRTX849 in Patients with Advanced Solid Tumors with KRAS G12C Mutation |
| Biomarkers: | KRAS G12C |
| Indication: | PDAC, Other Solid Tumors |
| Phase: | 1/2 |
| Treatment Line: | |
| Study Drug/Test Compound: | Adagrasib (MRTX849) |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
International Registry for Men With Advanced Prostate Cancer (IRONMAN) (IRONMAN)
| NCT#: & Link | NCT03151629 |
| NCT QR Code | ![]() |
| Available as of: | July 15, 2024 |
| Contract: | Caris |
| Indication Category: | Prostate |
| Study Sponsor: | PCCTC |
| Protocol #: | PRODIGY |
| Title: | International Registry for Men With Advanced Prostate Cancer (IRONMAN) (IRONMAN) |
| Highlight Details: | IRONMAN Registry Sub-Study: PRODIGY: Observational study to describe effectiveness of olaparib in subjects with metastatic castration-resistant prostate cancer who have failed prior treatment with a new hormonal agent and carry selected homologous recombination repair gene mutations |
| Biomarkers: | HRR mutations (BARD1, BRIP1, CHEK1, FANCL, PALB2, RAD51B, RAD51C, RAD51D, and RAD54L) |
| Indication: | Prostate (mCRPC) |
| Phase: | |
| Treatment Line: | |
| Study Drug/Test Compound: | |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
A Study of Zenocutuzumab (MCLA-128) in Patients With Solid Tumors Harboring an NRG1 Fusion (eNRGy)
| NCT#: & Link | NCT02912949 |
| NCT QR Code | ![]() |
| Available as of: | July 15 2024 |
| Contract: | Caris |
| Indication Category: | Solid Tumors |
| Study Sponsor: | Merus N.V. |
| Protocol #: | MCLA-128- CL01 |
| Title: | A Study of Zenocutuzumab (MCLA-128) in Patients With Solid Tumors Harboring an NRG1 Fusion (eNRGy) |
| Highlight Details: | ***REFERRAL ONLY*** A Study of Zenocutuzumab (MCLA- 128) in Patients With Solid Tumors Harboring an NRG1 Fusion (eNRGy) |
| Biomarkers: | NRG1 fusions |
| Indication: | Solid tumors |
| Phase: | 2 |
| Treatment Line: | |
| Study Drug/Test Compound: | MCLA-128 |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
Brightline-2: A Study to Test Whether Brigimadlin (BI 907828) Helps People With Cancer in the Biliary Tract, Pancreas, Lung or Bladder
| NCT#: & Link | NCT05512377 |
| NCT QR Code | ![]() |
| Available as of: | July 15 2024 |
| Contract: | Caris |
| Indication Category: | Solid Tumors |
| Study Sponsor: | Boehringer Ingelheim |
| Protocol #: | 1403-0011 |
| Title: | Brightline-2: A Study to Test Whether Brigimadlin (BI 907828) Helps People With Cancer in the Biliary Tract, Pancreas, Lung or Bladder |
| Highlight Details: | Brightline 2- A Phase II/III, open-label, single-arm, multi-centre trial of BI 907828 for treatment of patients with locally advanced/metastatic, MDM2 amplified, TP53 wild-type solid tumours-biliary tract adenocarcinoma, pancreatic ductal adenocarcinoma, or other selected solid tumors |
| Biomarkers: | MDM2 amplification |
| Indication: | Select solid tumors |
| Phase: | 2 |
| Treatment Line: | |
| Study Drug/Test Compound: | BI 907828 |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
A Study to Assess Disease Activity and Adverse Events of Intravenous (IV) Telisotuzumab Vedotin Compared to IV Docetaxel in Adult Participants With Previously Treated Non-Squamous Non-Small Cell Lung Cancer (NSCLC)
| NCT#: & Link | NCT04928846 |
| NCT QR Code | ![]() |
| Available as of: | July 15, 2024 |
| Contract: | Caris |
| Indication Category: | Lung |
| Study Sponsor: | AbbVie |
| Protocol #: | M18-868 |
| Title: | A Study to Assess Disease Activity and Adverse Events of Intravenous (IV) Telisotuzumab Vedotin Compared to IV Docetaxel in Adult Participants With Previously Treated Non-Squamous Non-Small Cell Lung Cancer (NSCLC) |
| Highlight Details: | **REFERRAL ONLY** A Phase 3 Open-Label, Randomized, Controlled, Global Study of Telisotuzumab Vedotin (ABBV- 399) Versus Docetaxel in Subjects With Previously Treated c-Met Overexpressing, EGFR Wildtype, Locally Advanced/Metastatic Non-Squamous Non-Small Cell Lung Cancer |
| Biomarkers: | c-MET |
| Indication: | NSCLC |
| Phase: | 3 |
| Treatment Line: | |
| Study Drug/Test Compound: | Telisotuzumab Vedotin (ABBV-399) |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
Study to Compare Furmonertinib to Platinum-Based Chemotherapy for Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) With Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertion Mutations (FURVENT)
| NCT#: & Link | NCT05607550 |
| NCT QR Code | ![]() |
| Available as of: | July 15 2024 |
| Contract: | Caris |
| Indication Category: | Lung |
| Study Sponsor: | ArriVent BioPharma |
| Protocol #: | FURMO-004 |
| Title: | Study to Compare Furmonertinib to Platinum-Based Chemotherapy for Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) With Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertion Mutations (FURVENT) |
| Highlight Details: | ***REFERRAL ONLY***A Global, Phase 3, Randomized, Multicenter, Open-Label Study to Investigate the Efficacy and Safety of Furmonertinib Compared to Platinum-Based Chemotherapy as First-Line Treatment for Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer with Epidermal Growth Factor Receptor Exon 20 Insertion Mutations |
| Biomarkers: | EGFR Exon 20 insertion mutation |
| Indication: | NSCLC |
| Phase: | 3 |
| Treatment Line: | |
| Study Drug/Test Compound: | Furmonertinib |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
Phase 2 Trial of Adagrasib Monotherapy and in Combination With Pembrolizumab and a Phase 3 Trial of Adagrasib in Combination in Patients With a KRAS G12C Mutation KRYSTAL-7
| NCT#: & Link | NCT04613596 |
| NCT QR Code | ![]() |
| Available as of: | July 15 2024 |
| Contract: | Caris |
| Indication Category: | Lung |
| Study Sponsor: | Mirati Therapeutics |
| Protocol #: | 849-007 |
| Title: | Phase 2 Trial of Adagrasib Monotherapy and in Combination With Pembrolizumab and a Phase 3 Trial of Adagrasib in Combination in Patients With a KRAS G12C Mutation KRYSTAL-7 |
| Highlight Details: | A Phase 2 Trial of Adagrasib Monotherapy and in Combination with Pembrolizumab and a Phase 3 Trial of Adagrasib in Combination with Pembrolizumab versus Pembrolizumab in Patients with Advanced Non-Small Cell Lung Cancer with KRAS G12C Mutation |
| Biomarkers: | KRAS G12C |
| Indication: | NSCLC |
| Phase: | 3 |
| Treatment Line: | |
| Study Drug/Test Compound: | Adagrasib |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
A Study to Assess the Efficacy and Safety of FORE8394 in Participants With Cancer Harboring BRAF Alterations
| NCT#: & Link | NCT05503797 |
| NCT QR Code | ![]() |
| Available as of: | October 2, 2024 |
| Contract: | Caris |
| Indication Category: | Brain/Spine |
| Study Sponsor: | Fore Biotherapeutics |
| Protocol #: | F8394-201: Subprotocol A & B |
| Title: | A Study to Assess the Efficacy and Safety of FORE8394 in Participants With Cancer Harboring BRAF Alterations |
| Highlight Details: | A Phase 2 Master Protocol to assess the efficacy and safety of FORE8394, an inhibitor of BRAF class 1 and class 2 alterations, in participants with cancer harboring BRAF alterations |
| Biomarkers: | BRAF Fusions/BRAF V600E |
| Indication: | Solid Tumors/CNS tumors |
| Phase: | 2 |
| Treatment Line: | |
| Study Drug/Test Compound: | FORE8394 |
| Notes | |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
Safety and Tolerability of TNG908 in Patients With MTAP-deleted Solid Tumors – Pancreatic
| NCT#: & Link | NCT05275478 |
| NCT QR Code | ![]() |
| Available as of: | July 3, 2024 |
| Contract: | Optimal |
| Indication Category: | Solid Tumors |
| Study Sponsor: | Tango Therapeutics |
| Protocol #: | TNG908- C101 |
| Title: | Safety and Tolerability of TNG908 in Patients With MTAP-deleted Solid Tumors A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG908 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors (TNG908-C101+J13) |
| Highlight Details: | • ECOG 0-1 • confirmed histologic or cytologic diagnosis of a locally advanced or metastatic solid tumor • Measurable disease based on RECIST, v1.1 • Documented bi-allelic (homozygous) deletion of MTAP in a tumor detected by a validated NGS test, or absence of MTAP protein in a tumor detected by a validated IHC test. • Adequate organ and hematological functions • Arm 4: Patients with locally advanced or metastatic pancreatic ductal adenocarcinoma • or adenosquamous carcinoma with predominantly adenocarcinoma histology • Progressive disease after prior treatment with standard of care therapy(ies) (eg, ESMO • At least 1 of the following criteria for standard-of-care therapy(ies): • a. Progression or an inadequate response to an approved standard-of-care therapy; there is no limit to the number of prior lines of therapy • b. No approved standard-of-care therapy • c. Patient is intolerant to the available standard-of-care therapy(ies) • d. Investigator has determined that treatment with the standard-of-care therapy is not appropriate |
| Biomarkers: | MTAP-deletion |
| Indication: | Pancreatic With MTAP deletion ARM 2 |
| Phase: | 2 |
| Treatment Line: | 2nd+ line |
| Study Drug/Test Compound: | TNG908 is a potent and selective oral small- molecule inhibitor of PRMT5. TNG908 binds cooperatively with MTA to inhibit PRMT5 function. Elevated levels of MTA are found in tumor cells that have lost the MTAP gene, which metabolizes MTA, conferring marked specificity of TNG908 for tumor cells that have lost MTAP but not normal cells |
| Notes | Phase 2 IP:TNG908 starting dose of 600mg BID PO |
| Recruitment Status: | Just In Time – PAUSED |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
Safety and Tolerability of TNG908 in Patients With MTAP-deleted Solid Tumors -Mesothelioma
| NCT#: & Link | NCT05275478 |
| NCT QR Code | ![]() |
| Available as of: | July 3, 2024 |
| Contract: | Optimal |
| Indication Category: | Solid Tumors |
| Study Sponsor: | Tango Therapeutics |
| Protocol #: | TNG908- C101 |
| Title: | Safety and Tolerability of TNG908 in Patients With MTAP-deleted Solid Tumors A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG908 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors (TNG908-C101+J13 |
| Highlight Details: | • ECOG 0-1 • confirmed histologic or cytologic diagnosis of a locally advanced or metastatic solid tumor • Measurable disease based on RECIST, v1.1 • Documented bi-allelic (homozygous) deletion of MTAP in a tumor detected by a validated NGS test, or absence of MTAP protein in a tumor detected by a validated IHC test. • Adequate organ and hematological functions • Arm 2: Patients with locally advanced or metastatic mesothelioma, or after following • local treatment guidelines (ie, ESMO guidelines) for the standard of care if more strict • Mesothelioma, any location • Progressive disease after prior treatment • At least 1 of the following criteria for standard-of-care therapy(ies): • a. Progression or an inadequate response to an approved standard-of-care therapy; there is no limit to the number of prior lines of therapy • b. No approved standard-of-care therapy • c. Patient is intolerant to the available standard-of-care therapy(ies) • d. Investigator has determined that treatment with the standard-of-care therapy is not appropriate |
| Biomarkers: | MTAP-deletion |
| Indication: | Mesothelioma With MTAP deletion ARM 2 |
| Phase: | 2 |
| Treatment Line: | 2nd+ line |
| Study Drug/Test Compound: | TNG908 is a potent and selective oral small- molecule inhibitor of PRMT5. TNG908 binds cooperatively with MTA to inhibit PRMT5 function. Elevated levels of MTA are found in tumor cells that have lost the MTAP gene, which metabolizes MTA, conferring marked specificity of TNG908 for tumor cells that have lost MTAP but not normal cells |
| Notes | Phase 2 IP:TNG908 starting dose of 600mg BID PO |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
Safety and Tolerability of TNG908 in Patients With MTAP-deleted Solid Tumors
| NCT#: & Link | NCT05275478 |
| NCT QR Code | ![]() |
| Available as of: | July 3, 2024 |
| Contract: | Optimal |
| Indication Category: | Solid Tumors |
| Study Sponsor: | Tango Therapeutics |
| Protocol #: | TNG908- C101 |
| Title: | Safety and Tolerability of TNG908 in Patients With MTAP-deleted Solid Tumors A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG908 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors (TNG908-C101+J13 |
| Highlight Details: | • ECOG 0-1 • confirmed histologic or cytologic diagnosis of a locally advanced or metastatic solid tumor • Measurable disease based on RECIST, v1.1 • Documented bi-allelic (homozygous) deletion of MTAP in a tumor detected by a validated NGS test, or absence of MTAP protein in a tumor detected by a validated IHC test. • Adequate organ and hematological functions • Arm 1: Patients with locally advanced or metastatic NSCLC (squamous or non-squamous) • Progressive disease after prior treatment or after following local treatment guidelines (ie, ESMO guidelines) for the standard of care if more strict. • Tested for known driver mutations/alterations (e.g., EGFR, ALK, and ROS1) and received at least 1 standard- of-care targeted therapy(ies) for the known alteration, if present or after failing local treatment guidelines (ie, ESMO or trial guidelines) for the standard of care if more strict • At least 1 of the following criteria for standard-of-care therapy(ies): • a. Progression or an inadequate response to an approved standard-of-care therapy; there is no limit to the number of prior lines of therapy • b. No approved standard-of-care therapy • c. Patient is intolerant to the available standard-of-care therapy(ies) • d. Investigator has determined that treatment with the standard-of-care therapy is not appropriate |
| Biomarkers: | MTAP-deletion |
| Indication: | Lung NSCLC With MTAP deletion ARM 1 |
| Phase: | 2 |
| Treatment Line: | 2nd+ line |
| Study Drug/Test Compound: | TNG908 is a potent and selective oral small- molecule inhibitor of PRMT5. TNG908 binds cooperatively with MTA to inhibit PRMT5 function. Elevated levels of MTA are found in tumor cells that have lost the MTAP gene, which metabolizes MTA, conferring marked specificity of TNG908 for tumor cells that have lost MTAP but not normal cells |
| Notes | Phase 2 IP:TNG908 starting dose of 600mg BID PO |
| Recruitment Status: | Just In Time |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
NRG-BR009 – Evaluating the Addition of Adjuvant Chemotherapy to Ovarian Function Suppression Plus Endocrine Therapy in Premenopausal Patients With pN0-1, ER-Positive/HER2-Negative Breast Cancer and an Oncotype Recurrence Score Less Than or Equal to 25 (OFSET)
| NCT#: | NCT05879926 |
| NCT QR Code | ![]() |
| Title: | NRG-BR009 – Evaluating the Addition of Adjuvant Chemotherapy to Ovarian Function Suppression Plus Endocrine Therapy in Premenopausal Patients With pN0-1, ER-Positive/HER2-Negative Breast Cancer and an Oncotype Recurrence Score Less Than or Equal to 25 (OFSET) |
| Protocol: | NRG-BR009 |
| Cancer Type: | Breast |
| Study Sponsor: | NRG Oncology |
| Brief Summary: | This Phase III Trial will determine whether adjuvant chemotherapy (ACT) added to ovarian function suppression (OFS) plus endocrine therapy (ET) is superior to OFS plus ET in improving invasive breast cancer-free survival (IBCFS) among premenopausal, early- stage breast cancer (EBC) patients with estrogen receptor (ER)-positive, HER2-negative tumors and 21-gene recurrence score (RS) between 16-25 (for pN0 patients) and 0-25 (for pN1 patients). |
| Study Type: | Intervention |
| Date Opened at SVH: | March 12, 2024 |
| Recruitment Status: | Recruiting |
| Study Population: | See SCHEMA |
| Eligibility Criteria: | See SCHEMA |
| Principal Investigators: | Geetha N. Varma, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 Hong Zhao, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
| Link to ClinicalTrials.gov | https://clinicaltrials.gov/study/NCT05879926?term=NCT05879926&limit=10&rank=1 |
| Summary | See Physician Material See Patient-facing Material |
Observational Basket Trial to Collect Tissue to Train and Validate a Live Tumor Diagnostic Platform (CYBRID-02)
| NCT#: | NCT05520099 |
| NCT QR Code | ![]() |
| Title: | Observational Basket Trial to Collect Tissue to Train and Validate a Live Tumor Diagnostic Platform (CYBRID-02) |
| Protocol: | CYBRID-02 |
| Cancer Type: | multiple |
| Study Sponsor: | Elephas |
| Brief Summary: | The primary objective of this study is to determine the ex-vivo prognostic accuracy of the Cybrid live tumor diagnostic platform across a basket of solid tumors, using in-vivo RECIST 1.1 as the reference method. |
| Study Type: | Intervention/Treatment |
| Date Opened at SVH: | February 21, 2024 |
| Recruitment Status: | closed |
| Study Population: | See SCHEMA |
| Eligibility Criteria: | See SCHEMA |
| Principal Investigators: | Geetha N. Varma, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 Hong Zhao, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
| Link to ClinicalTrials.gov | https://clinicaltrials.gov/study/NCT05520099?term=elephas%20cybrid&rank=2 |
| Summary | See Patient-Facing Material |
S2212 – Shorter Anthracycline-Free Chemo Immunotherapy Adapted to Pathological Response in Early Triple Negative Breast Cancer (SCARLET), A Randomized Phase III Study
| NCT#: | NCT05929768 |
| NCT QR Code | ![]() |
| Title: | Shorter Anthracycline-Free Chemo Immunotherapy Adapted to Pathological Response in Early Triple Negative Breast Cancer (SCARLET), A Randomized Phase III Study |
| Protocol: | S2212 |
| Cancer Type | Breast |
| Study Sponsor: | SWOG Cancer Research Network |
| Brief Summary: | This phase III trial compares the effects of shorter chemotherapy (chemo)-immunotherapy without anthracyclines to usual chemo-immunotherapy for the treatment of early-stage triple negative breast cancer. Paclitaxel is in a class of medications called anti-microtubule agents. It stops cancer cells from growing and dividing and may kill them. Carboplatin is in a class of medications known as platinum-containing compounds. It works in a way similar to the anticancer drug cisplatin, but may be better tolerated than cisplatin. Carboplatin works by killing, stopping or slowing the growth of cancer cells. Cyclophosphamide is in a class of medications called alkylating agents. It works by damaging the cell’s deoxyribonucleic acid (DNA) and may kill cancer cells. It may also lower the body’s immune response. Docetaxel is in a class of medications called taxanes. It stops cancer cells from growing and dividing and may kill them. Doxorubicin is an anthracycline chemotherapy drug that damages DNA and may kill cancer cells. Pembrolizumab may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Shorter treatment without anthracycline chemotherapy may work the same as the usual anthracycline chemotherapy treatment for early-stage triple negative breast cancer. |
| Study Type: | Interventional |
| Date Opened at SVH: | February 7, 2024 |
| Recruitment Status: | Recruiting |
| Study Population: | |
| Eligibility Criteria: | See SCHEMA |
| Principal Investigator: | Geetha N. Varma, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
| Link to ClinicalTrials.gov | https://classic.clinicaltrials.gov/ct2/show/NCT05812807?term=NCT05812807&draw=2&rank=1 |
| Summary | Summary |
A012103 – Pembrolizumab vs. Observation in People With Triple-negative Breast Cancer Who Had a Pathologic Complete Response After Chemotherapy Plus Pembrolizumab
| NCT#: | NCT05812807 |
| NCT QR Code | ![]() |
| Title: | OptimICE-PCR: De-Escalation of Therapy in Early-Stage TNBC Patients Who Achieve pCR After Neoadjuvant Chemotherapy With Checkpoint Inhibitor Therapy |
| Protocol: | A012103 |
| Cancer Type | Breast |
| Study Sponsor: | Alliance/NCI |
| Brief Summary: | The phase III trial compares the effect of pembrolizumab to observation for the treatment of patients with early-stage triple-negative breast cancer who achieved a pathologic complete response after preoperative chemotherapy in combination with pembrolizumab. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body’s immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. This trial may help researchers determine if observation will result in the same risk of cancer coming back as pembrolizumab after surgery in triple-negative breast cancer patients who achieve pathologic complete response after preoperative chemotherapy with pembrolizumab. |
| Study Type: | Interventional |
| Date Opened at SVH: | August 3, 2023 |
| Recruitment Status: | Recruiting |
| Study Population: | |
| Eligibility Criteria: | See SCHEMA |
| Principal Investigator: | Geetha N. Varma, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
| Link to ClinicalTrials.gov | https://classic.clinicaltrials.gov/ct2/show/NCT05812807?term=NCT05812807&draw=2&rank=1 |
| Schema | Schema |
NRG-GI008 – Colon Adjuvant Chemotherapy Based on Evaluation of Residual Disease (CIRCULATE-US)
| NCT#: | NCT05174169 |
| NCT QR Code | ![]() |
| Title: | NRG-GI008 – Colon Adjuvant Chemotherapy Based on Evaluation of Residual Disease (CIRCULATE-US) |
| Protocol: | NRG-GI008 |
| Cancer Type: | Colon Cancer |
| Study Sponsor: | NRG Oncology |
| Brief Summary: | This Phase II/III trial will evaluate the what kind of chemotherapy to recommend to patients based on the presence or absences of circulating tumor DNA (ctDNA) after surgery for colon cancer. |
| Study Type: | Interventional |
| Date Opened at SVH: | opening soon |
| Recruitment Status: | opening soon |
| Study Population: | |
| Eligibility Criteria: | See SCHEMA |
| Principal Investigator: | Geetha N. Varma, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
| Link to ClinicalTrials.gov: | https://clinicaltrials.gov/ct2/show/study/NCT05174169 |
| Schema | Schema |
A022104 – Testing the Addition of an Anti-Cancer Drug, Irinotecan, to the Standard Chemotherapy Treatment (FOLFOX) After Long-Course Radiation Therapy for Advanced-Stage Rectal Cancers to Improve the Rate of Complete Response and Long-Term Rates of Organ Preservation (JANUS)
| NCT#: | NCT05610163 |
| NCT QR Code | ![]() |
| Title: | A022104 – Testing the Addition of an Anti-Cancer Drug, Irinotecan, to the Standard Chemotherapy Treatment (FOLFOX) After Long-Course Radiation Therapy for Advanced-Stage Rectal Cancers to Improve the Rate of Complete Response and Long-Term Rates of Organ Preservation (JANUS) |
| Protocol: | A022104 |
| Cancer Type: | Rectal Cancer |
| Study Sponsor: | Alliance/NCI |
| Brief Summary: | This phase II trial compares the effect of irinotecan versus oxaliplatin after long-course chemoradiation in patients with stage II-III rectal cancer. Combination chemotherapy drugs, such as FOLFIRINOX (fluorouracil, irinotecan, leucovorin, and oxaliplatin), FOLFOX (leucovorin, fluorouracil, oxaliplatin, and irinotecan ), and CAPOX (capecitabin and oxaliplatin) work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. FOLFOX or CAPOX are used after chemoradiation as usual treatment for rectal cancer. Giving FOLFIRINOX after chemoradiation may increase the response rate and lead to higher rates of clinical complete response (with a chance of avoiding surgery) compared to FOLFOX or CAPOX after chemoradiation in patients with locally advanced rectal cancer. |
| Study Type: | Interventional |
| Date Opened at SVH: | February 15, 2022 |
| Recruitment Status: | Closed |
| Study Population: | |
| Eligibility Criteria: | See SCHEMA |
| Principal Investigator: | Geetha N. Varma, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
| Link to ClinicalTrials.gov: | https://clinicaltrials.gov/ct2/show/record/NCT05610163?term=A022104&draw=2&rank=1 |
| Schema | Schema |
CCTG MA.39 – Regional Radiotherapy in Biomarker Low-Risk Node Positive and T3N0 Breast Cancer (TAILOR RT)
| NCT#: | NCT03488693 |
| NCT QR Code | ![]() |
| Title: | Regional Radiotherapy in Biomarker Low-Risk Node Positive and T3N0 Breast Cancer (TAILOR RT) |
| Protocol: | CCTG MA.39 |
| Cancer Type: | Breast |
| Study Sponsor: | Canadian Cancer Trials Group NCI CIRB |
| Brief Summary: | The purpose of this study is to compare the effects on low risk breast cancer receiving usual care that includes regional radiation therapy, with receiving no regional radiation therapy. Researchers want to see if not giving this type of radiation treatment works as well at preventing breast cancer from coming back. |
| Study Type: | Interventional |
| Date Opened at SVH: | May 6, 2022 |
| Recruitment Status: | Recruiting |
| Study Population: | |
| Eligibility Criteria: | See SCHEMA |
| Principal Investigator: | Jacob Andrade MD PhD, Coastal Radiation Oncology Salinas, (831) 758-2724 |
| Participating Institution: | Salinas Valley Health |
| SVH Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, research@salinasvalleyhealth.com |
| Link to ClinicaTrials.gov | https://clinicaltrials.gov/ct2/show/record/NCT03488693?term=CCTG+MA.3&draw=2&rank=1 |
| Schema | Schema |
A082002 – Testing the Addition of Radiation Therapy to the Usual Treatment (Immunotherapy With or Without Chemotherapy) for Stage IV Non-Small Cell Lung Cancer Patients Who Are PD-L1 Negative
| NCT#: | NCT04929041 |
| NCT QR Code | ![]() |
| Title: | A082002 – Testing the Addition of Radiation Therapy to the Usual Treatment (Immunotherapy With or Without Chemotherapy) for Stage IV Non-Small Cell Lung Cancer Patients Who Are PD-L1 Negative |
| Protocol: | A082002 |
| Cancer Type: | Lung Cancer |
| Study Sponsor: | Alliance/NCI |
| Brief Summary: | This phase II/III trial compares the addition of radiation therapy to the usual treatment (immunotherapy with or without chemotherapy) vs. usual treatment alone in treating patients with non-small cell lung cancer that has spread to nearby tissue or lymph nodes (advanced) or has spread to other places in the body (metastatic) whose tumor is also negative for a molecular marker called PD-L1. Stereotactic body radiation therapy (SBRT) is a type of radiation therapy that uses high energy x-rays to kill tumor cells and shrink tumors. This method uses special equipment to position a patient and precisely deliver radiation to tumors with fewer doses over a shorter period and may cause less damage to normal tissue than conventional radiation therapy. Immunotherapy with monoclonal antibodies, such as nivolumab, ipilimumab and pembrolizumab, may help the body’s immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Chemotherapy drugs, such as carboplatin, pemetrexed, paclitaxel and nab-paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. The addition of radiation therapy to usual treatment may stop the cancer from growing and increase the life of patients with advanced non-small cell lung cancer who are PD-L1 negative. |
| Study Type: | Interventional |
| Date Opened at SVH: | April 14, 2022 |
| Recruitment Status: | closed |
| Study Population: | |
| Eligibility Criteria: | See Schema |
| Principal Investigator: | Hong Zhao, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Health |
| SVH Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, Research@SalinasValleyHealth.com |
| Link to ClinicalTrials.gov: | https://clinicaltrials.gov/ct2/show/record/NCT04929041?term=a082002&draw=2&rank=1 |
| Schema | Schema |
A011801 – T-DM1 and Tucatinib Compared With T-DM1 Alone in Preventing Relapses in People With High Risk HER2-Positive Breast Cancer, the CompassHER2 RD Trial
| NCT# | NCT04457596 |
| NCT QR Code | ![]() |
| Title: | T-DM1 and Tucatinib Compared With T-DM1 Alone in Preventing Relapses in People With High Risk HER2-Positive Breast Cancer, the CompassHER2 RD Trial |
| Protocol: | A011801 |
| Cancer Type: | Breast |
| Study Sponsor: | NCI /Alliance |
| Brief Summary: | This phase III trial studies how well trastuzumab emtansine (T-DM1) and tucatinib work in preventing breast cancer from coming back (relapsing) in patients with high risk, HER2 positive breast cancer. T-DM1 is a monoclonal antibody, called trastuzumab, linked to a chemotherapy drug, called DM1. Trastuzumab is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as HER2 receptors, and delivers DM1 to kill them. Tucatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving T-DM1 and tucatinib may work better in preventing breast cancer from relapsing in patients with HER2 positive breast cancer compared to T-DM1 alone. |
| Study Type: | Interventional |
| Date Opened at SVH: | 4-Jan-2022 |
| Recruitment Status: | Closed |
| Study Population: | |
| Eligibility Criteria: | See SCHEMA |
| Principal Investigator: | Hong Zhao, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Health |
| SVH Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, Research@SalinasValleyHealth.com |
| Link to ClinicalTrials.gov: | https://clinicaltrials.gov/ct2/show/record/NCT04457596?term=A011801&draw=2&rank=1 |
| Schema & Protocol | A011801-Schema |
EA2183 – Testing the Addition of Radiotherapy to the Usual Treatment (Chemotherapy) for Patients With Esophageal and Gastric Cancer That Has Spread to a Limited Number of Other Places in the Body
| NCT#: | NCT04248452 |
| NCT QR Code | ![]() |
| Title: | Testing the Addition of Radiotherapy to the Usual Treatment (Chemotherapy) for Patients With Esophageal and Gastric Cancer That Has Spread to a Limited Number of Other Places in the Body |
| Protocol: | EA2183 |
| Cancer Type: | Esophageal/Gastric |
| Study Sponsor: | NCI / ECOG-ACRIN |
| Brief Summary: | This phase III trial studies how well the addition of radiotherapy to the usual treatment (chemotherapy) works compared to the usual treatment alone in treating patients with esophageal and gastric cancer that has spread to a limited number of other places in the body (oligometastatic disease). Radiotherapy uses high energy x-rays, gamma rays, or protons to kill tumor cells and shrink tumors. Drugs used in usual chemotherapy, such as leucovorin, 5-fluorouracil, oxaliplatin, and capecitabine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Adding radiotherapy to the usual chemotherapy may work better compared to the usual chemotherapy alone in treating patients with esophageal and gastric cancer. |
| Study Type: | Interventional |
| Date Opened at SVH: | 2-Sep-2021 |
| Recruitment Status: | Closed to Recruiting |
| Study Population: | |
| Eligibility Criteria: | See Schema |
| Principal Investigator: | Hong Zhao, MD, Oncology, Salinas Valley Health Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Health |
| Salinas Valley Health Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, Research@SalinasValleyHealth.com |
| Link to ClinicalTrials.gov: | https://clinicaltrials.gov/ct2/show/record/NCT04248452?term=EA2183&draw=2&rank=1 |
| Physician Fact Sheet: | EA2183 Schema |
EA5182 – Osimertinib With or Without Bevacizumab as Initial Treatment for Patients With EGFR-Mutant Lung Cancer
| NCT#: | NCT04181060 |
| NCT QR Code | ![]() |
| Title: | Osimertinib With or Without Bevacizumab as Initial Treatment for Patients With EGFR-Mutant Lung Cancer |
| Protocol: | EA5182 |
| Cancer Type: | Lung |
| Study Sponsor: | NCI / ECOG-ACRIN |
| Brief Summary: | This phase III trial compares the effect of bevacizumab and osimertinib combination vs. osimertinib alone for the treatment of non-small cell lung cancer that has spread outside of the lungs (stage IIIB-IV) and has a change (mutation) in a gene called EGFR. The EGFR protein is involved in cell signaling pathways that control cell division and survival. Sometimes, mutations in the EGFR gene cause EGFR proteins to be made in higher than normal amounts on some types of cancer cells. This causes cancer cells to divide more rapidly. Osimertinib may stop the growth of tumor cells by blocking EGFR that is needed for cell growth in this type of cancer. Monoclonal antibodies, such as bevacizumab, may interfere with the ability of tumor cells to grow and spread. Giving osimertinib with bevacizumab may control cancer for longer and help patients live longer as compared to osimertinib alone. |
| Study Type: | Interventional |
| Date Opened at SVH: | 2-Sep-2021 |
| Recruitment Status: | Closed |
| Study Population: | |
| Eligibility Criteria: | See SCHEMA |
| Principal Investigator: | Hong Zhao, MD, Oncology, SVMC Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Memorial Healthcare System & Salinas Valley Medical Clinics & Salinas Valley Memorial Hospital |
| SVH Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, Research@SalinasValleyHealth.com |
| Link to ClinicalTrials.gov: | https://clinicaltrials.gov/ct2/show/record/NCT04181060?term=EA5182&draw=2&rank=1 |
| Physician Fact Sheet: | EA5182 SCHEMA |
Doxorubicin Hydrochloride and Cyclophosphamide Followed by Paclitaxel With or Without Carboplatin in Treating Patients With Triple-Negative Breast Cancer
| NCT#: | NCT02488967 |
| NCT QR Code | ![]() |
| Title: | Doxorubicin Hydrochloride and Cyclophosphamide Followed by Paclitaxel With or Without Carboplatin in Treating Patients With Triple-Negative Breast Cancer |
| Protocol: | NRG-BR003 |
| Cancer Type: | Breast |
| Study Sponsor: | NCI / ECOG-ACRIN |
| Brief Summary: | This randomized phase III trial studies how well doxorubicin hydrochloride and cyclophosphamide followed by paclitaxel with or without carboplatin work in treating patients with triple-negative breast cancer. Drugs used in chemotherapy, such as doxorubicin hydrochloride, cyclophosphamide, paclitaxel, and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. It is not yet known whether doxorubicin hydrochloride and cyclophosphamide is more effective when followed by paclitaxel alone or paclitaxel and carboplatin in treating triple-negative breast cancer. |
| Study Type: | Interventional |
| Date Opened at SVMHS: | 28-Jan-2016 |
| Recruitment Status: | Closed |
| Study Population: | |
| Eligibility Criteria: | The tumor must be unilateral invasive adenocarcinoma of the breast on histologic examination |
| Principal Investigator: | Hong Zhao, MD, Oncology, SVMC Cancer Care, (831) 755-1701 |
| Participating Institution: | Salinas Valley Memorial Healthcare System & Salinas Valley Medical Clinics & Salinas Valley Memorial Hospital |
| SVMHS Clinical Research Program: | Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager, tnielsen2@svmh.com |
| Link to ClinicalTrials.gov: | https://clinicaltrials.gov/ct2/show/record/NCT02488967?term=NRG-BR003&draw=2&rank=1 |




























