A Study of INCMGA00012 in Squamous Carcinoma of the Anal Canal Following Platinum-Based Chemotherapy (POD1UM-202)

• Status: Active, not recruiting
• Trial end date: 2022-02-17
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to assess the efficacy of INCMGA00012 in participants with locally advanced or metastatic squamous carcinoma of the anal canal (SCAC) who have progressed after platinum-based chemotherapy.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Incyte Corporation
• Treatments: Antibodies

Criteria

Inclusion Criteria:

• Ability to comprehend and willingness to sign a written informed consent form.

• Confirmed diagnosis of locally advanced or metastatic SCAC.

• Must have received (or been intolerant to or ineligible for) at least 1 prior line of platinum-based chemotherapy and received no more than 2 prior systemic treatments.

• Must have measurable disease by RECIST v1.1.

• Eastern Cooperative Oncology Group performance status of 0 to 1.

• If HIV-positive, then all of the following criteria must also be met: CD4+ count ≥ 300/μL, undetectable viral load, and receiving highly active antiretroviral therapy.

Exclusion Criteria:

• Receipt of anticancer therapy or participation in another interventional clinical study within 21 days before the first administration of study drug; 6 weeks for mitomycin C.

• Radiotherapy within 14 days of first dose of study treatment with the following caveats: 28 days for pelvic radiotherapy, 6 months for thoracic region radiotherapy that is > 30 Gy.

• Prior treatment with programmed cell death protein 1 (PD-1) or programmed cell death ligand protein 1 (PD-L1)-directed therapy.

• Active autoimmune disease requiring systemic immunosuppression.

• Known central nervous system (CNS) metastases and/or carcinomatous meningitis.

• Known active hepatitis infection.

• Active infections requiring systemic therapy.

• Is pregnant or breastfeeding or is expecting to conceive or father children within the projected duration of the study, from screening through 6 months after the last dose of study drug.