NRG-CC015: Harnessing E-Mindfulness Approaches for Living After Breast Cancer (HEAL-ABC)

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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

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 

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NCT#: & LinkNCT05578092
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

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NCT#: & LinkNCT05732831
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
Notes462 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

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NCT#: & LinkNCT04094610
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
NotesPhase 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

Phase 1/​2 Study of MRTX849 in Patients With Cancer Having a KRAS G12C Mutation KRYSTAL-1

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NCT#: & LinkNCT03785249
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)

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NCT#: & LinkNCT03151629
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)

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NCT#: & LinkNCT02912949
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

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NCT#: & LinkNCT05512377
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)

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NCT#: & LinkNCT04928846
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)

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NCT#: & LinkNCT05607550
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

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NCT#: & LinkNCT04613596
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

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NCT#: & LinkNCT05503797
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

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NCT#: & LinkNCT05275478
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
NotesPhase 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

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NCT#: & LinkNCT05275478
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
NotesPhase 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

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NCT#: & LinkNCT05275478
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
NotesPhase 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)

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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.govhttps://clinicaltrials.gov/study/NCT05879926?term=NCT05879926&limit=10&rank=1
SummarySee Physician Material
See Patient-facing Material

Observational Basket Trial to Collect Tissue to Train and Validate a Live Tumor Diagnostic Platform (CYBRID-02)

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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.govhttps://clinicaltrials.gov/study/NCT05520099?term=elephas%20cybrid&rank=2
SummarySee 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

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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 TypeBreast
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.govhttps://classic.clinicaltrials.gov/ct2/show/NCT05812807?term=NCT05812807&draw=2&rank=1
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A012103 – Pembrolizumab vs. Observation in People With Triple-negative Breast Cancer Who Had a Pathologic Complete Response After Chemotherapy Plus Pembrolizumab

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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 TypeBreast
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.govhttps://classic.clinicaltrials.gov/ct2/show/NCT05812807?term=NCT05812807&draw=2&rank=1
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NRG-GI008 – Colon Adjuvant Chemotherapy Based on Evaluation of Residual Disease (CIRCULATE-US)

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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
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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)

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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
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CCTG MA.39 – Regional Radiotherapy in Biomarker Low-Risk Node Positive and T3N0 Breast Cancer (TAILOR RT)

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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.govhttps://clinicaltrials.gov/ct2/show/record/NCT03488693?term=CCTG+MA.3&draw=2&rank=1
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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

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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
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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

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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
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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

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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
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EA5182 – Osimertinib With or Without Bevacizumab as Initial Treatment for Patients With EGFR-Mutant Lung Cancer

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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

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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