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Phase 2 N=94 Treatment

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

Squamous Cell Carcinoma of Anal Canal

Enrolled (actual)
94
Serious AEs
53.2%
Results posted
Aug 2021
Primary outcome: Primary: Objective Response Rate (ORR) — 13.8 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Retifanlimab (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Incyte Corporation
Primary completion
Jun 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Objective Response Rate (ORR)
13.8
SECONDARY
Duration of Response (DOR)
9.5
SECONDARY
Disease Control Rate (DCR)
48.9
SECONDARY
Progression-free Survival (PFS)
2.3
SECONDARY
Overall Survival
13.4
SECONDARY
Number of Participants With Treatment-emergent Adverse Events (TEAEs)
90
SECONDARY
Cmax of Retifanlimab
151
SECONDARY
Tmax of Retifanlimab
1.20
SECONDARY
Cmin of Retifanlimab
22.4
SECONDARY
AUC0-t of Retifanlimab
1950

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.

Eligibility 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.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03597295). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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