About the study

This is a phase 1/2 open label sequential dose escalation and cohort expansion study evaluating the safety, tolerability and preliminary antitumor activity of COM701 in combination with BMS-986207 and nivolumab in patients with advanced solid tumors.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria

1. Histologically or cytologically confirmed, locally advanced or metastatic solid malignancy and has exhausted all available standard therapy or is not a candidate for the available standard therapy.
2. Eastern Cooperative Oncology Group (ECOG) performance status 0-1.
3. During dose escalation
4. Subjects who received prior therapy with anti-PD-1, anti-PD-L1, anti
5. CTLA-4, OX-40, CD137, etc., are eligible. During cohort expansion: All subjects must have measurable disease as defined by RECIST v1.1. Expansion Cohorts:
6. Cohort 1 (subjects with advanced epithelial ovarian, fallopian tube, or primary peritoneal carcinoma)
7. Subject must have platinum refractory/resistant ovarian cancer defined as refractoriness to platinum-containing regimen or disease recurrence < 6 months after completion of a platinum-containing regimen
8. Cohort 2 (endometrial cancer cohort)
9. Subjects with locally advanced or metastatic microsatellite stable endometrial cancer with disease recurrence or progression during or after prior therapy that included platinum-based chemotherapy.
10. Subjects must have documented MSS status by an approved test e.g. genomic testing, IHC for mismatch repair proficient.
11. Subjects must have received no more than 2 prior systemic cytotoxic therapies; there are no limits to the number of prior endocrine or antiangiogenic regimens
12. Cohort 3 (basket cohort, excludes tumor types in cohorts 1 and 2)
13. Tumor types with high expression of PVRL2 (determined by central testing).
14. Cohort 4 (Head and Neck cancer)
15. Histologically confirmed recurrent or metastatic HNSCC (oral cavity, oropharynx, larynx, hypopharynx, nasopharynx, paranasal sinus, nasopharyngeal)
16. Cohort 4a
17. IO naïve. Eligible subjects can be systemic therapy naïve (frontline) or platinum failure.
18. Cohort 4b
19. IO failure. No limitations on the number of prior lines of systemic therapy. Key

Exclusion criteria

1. Active autoimmune disease requiring systemic therapy in the last 2 years prior to the first dose of COM701.
2. Symptomatic interstitial lung disease or inflammatory pneumonitis.
3. History of immune-related events that lead to immunotherapy treatment discontinuation.
4. Untreated or symptomatic central nervous system (CNS) metastases. Key Exclusion Criteria For Dose Expansion Cohorts:
5. Cohort 1: Prior therapy with an anti-PD-1/PD-L1/2, COM701 (or any inhibitor of PVRIG), anti-TIGIT antibody, anti-CTLA-4 antibody, anti-OX-40 antibody, anti-CD137 antibody.
6. Cohort 2: Prior therapy with COM701 (or any inhibitor of PVRIG) or anti-TIGIT antibody. Subjects with MSI-H endometrial cancer are ineligible.
7. Cohort 3: Prior therapy with COM701 (or any inhibitor of PVRIG) or anti-TIGIT antibody are ineligible.
8. Cohort 4: Subjects who have received prior therapy with COM701 (or any inhibitor of PVRIG), anti-TIGIT antibody, anti-CTLA-4 antibody, anti-OX-40 antibody, anti-CD137 antibody. Subjects in cohort 4a must be IO-naïve.

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

Determine if a study site for this clinical trial is near you. Contact the study to apply.