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 of Repotrectinib in Pediatric and Young Adult Subjects Harboring ALK, ROS1, OR NTRK1-3 Alterations

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, [email protected]

The Caris Biorepository Research Protocol

NCT#: & LinkNCT01499394
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, [email protected]

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

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, [email protected]

International Registry for Men With Advanced Prostate Cancer (IRONMAN) (IRONMAN)

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, [email protected]

A Study of Zenocutuzumab (MCLA-128) in Patients With Solid Tumors Harboring an NRG1 Fusion (eNRGy)

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, [email protected]

Brightline-2: A Study to Test Whether Brigimadlin (BI 907828) Helps People With Cancer in the Biliary Tract, Pancreas, Lung or Bladder

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, [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]

A Study to Assess the Efficacy and Safety of FORE8394 in Participants With Cancer Harboring BRAF Alterations

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, [email protected]

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

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, [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]