No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
150 (estimated)
Sponsor
Verastem, Inc. · Industry
Who this trial is looking for
This trial is looking for patients with a specific type of colorectal cancer called KRAS G12D-mutated metastatic colorectal cancer. Participants will receive the drug VS-7375, and possibly other treatments, to see how well it works and how safe it is.
Are You a Good Fit for This Trial?
You may be able to join if
I have metastatic colorectal cancer confirmed by a doctor.
I have measurable disease as per RECIST 1.1 criteria.
I have a confirmed KRAS G12D mutation from local testing.
My ECOG performance status is 0 or 1.
I have received at least one standard chemotherapy for my colorectal cancer and my disease has gotten worse after that.
I have stable disease, a partial response, or a complete response in my past treatment.
I have not received any treatment for my metastatic cancer or have had no more than one cycle of treatment.
You may not be able to join if
I have any other known RAS mutations.
I received anti-cancer treatment within the last 4 weeks.
I had major surgery within the last 4 weeks.
I had radiation therapy within the last week.
I have taken a direct RAS inhibitor before.
I have received more than one investigational therapy.
I have untreated or symptomatic brain metastasis.
I cannot swallow oral medication.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
This study will assess the safety and efficacy of VS-7375 alone and in combination with cetuximab or panitumumab and cetuximab plus mFOLFOX in patients with metastatic KRAS G12D - mutated Colorectal Cancer
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* Histopathology confirmed metastatic CRC
* Measurable disease per RECIST 1.1
* Local testing confirmed KRAS G12D mutation (tissue required for confirmatory central testing)
* ECOG PS=0 or 1
2L+ patients:
* Must have received at least 1 standard chemotherapy for metastatic co…
Inclusion Criteria:
* Histopathology confirmed metastatic CRC
* Measurable disease per RECIST 1.1
* Local testing confirmed KRAS G12D mutation (tissue required for confirmatory central testing)
* ECOG PS=0 or 1
2L+ patients:
* Must have received at least 1 standard chemotherapy for metastatic colorectal adenocarcinoma
* Have documented disease progression during or following their most recent prior line of therapy
* Have either stable disease, partial response (PR), or complete response (CR) by RECIST v1.1 as the best overall response (BOR) during at least 1 prior systemic therapy.
1L patients:
* Treatment-naïve or received no more than 1 cycle of standard systemic therapy for metastatic disease.
Exclusion Criteria:
* Have any other documented co-existing common RAS mutation(s)
* Prior anti-cancer Tx within 4 weeks or drug-specific timeline within first treatment dose, whichever shorter
* Major surgery within 4 weeks of first treatment dose
* Radiation therapy (RT) within 1 week of first treatment dose
* Receipt of prior direct RAS inhibitor
* Receipt of more than 1 investigational therapy
* Untreated or symptomatic CNS metastasis
* Receipt of strong CYP3A4 inhibitor/inducer or CYP3A4 sensitive substrates with narrow therapeutic index within 14 days or drug-specific timeline within first treatment dose, whichever is shorter
* Receipt of PPI or H2 blocker within 5 days
* Inability to swallow oral medication
* Other protocol-defined inclusion/exclusion criteria may apply
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