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#: & 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, [email protected]

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#: & 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, [email protected]

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#: & 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, [email protected]

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#: & 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, [email protected]

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#: & 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, [email protected]

Safety and Tolerability of TNG908 in Patients With MTAP-deleted Solid Tumors -Mesothelioma

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, [email protected]

Safety and Tolerability of TNG908 in Patients With MTAP-deleted Solid Tumors

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, [email protected]

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: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, [email protected]
Link to ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT05520099?term=elephas%20cybrid&rank=2
SummarySee Patient-Facing Material

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:  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
SVH Clinical Research Program:  Terri Nielsen, MSJ, RN, CCRP, Clinical Research Program Manager,  [email protected]
Link to ClinicalTrials.gov:  https://clinicaltrials.gov/ct2/show/record/NCT04929041?term=a082002&draw=2&rank=1
SchemaSchema

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:  Recruiting
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,  [email protected]
Link to ClinicalTrials.gov:  https://clinicaltrials.gov/ct2/show/record/NCT04181060?term=EA5182&draw=2&rank=1
Physician Fact Sheet:EA5182
SCHEMA