INCAGN01876 in Combination With Immunotherapy in Participants With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

Sponsor

Incyte Biosciences International Sàrl (Industry)

Overall Status

Not yet recruiting

CT.gov ID

NCT05359692

Collaborator

(none)

Enrollment

Arms

26.6

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the safety, tolerability, efficacy, PK and pharmacodynamics of INCAGN01876 when given in combination with retifanlimab. The study will consist of 2 parts: a safety lead-in part (Part 1) followed by a dose expansion part (Part 2).

Condition or Disease	Intervention/Treatment	Phase
Recurrent Cancer Metastatic Cancer Advanced Malignancies Head and Neck Squamous Cell Carcinoma	Biological: INCAGN01876 Biological: retifanlimab	Phase 2

Detailed Description

The purpose of this study is to determine the safety, tolerability, efficacy, PK and pharmacodynamics of INCAGN01876 when given in combination with retifanlimab in participants with GITR expression in recurrent or metastatic HNSCC who have progressed on or after prior systemic therapy including anti-PD-(L)1 therapy. The study will consist of 2 parts: a safety lead-in part (Part 1) followed by a dose expansion part (Part 2)

Study Design

Study Type:

Interventional

Anticipated Enrollment :

50 participants

Allocation:

Non-Randomized

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Masking Description:

open-label study

Primary Purpose:

Treatment

Official Title:

Phase 2, Open-Label, Multicenter Study of INCAGN01876 in Combination With Immunotherapy in Participants With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

Anticipated Study Start Date :

Sep 19, 2022

Anticipated Primary Completion Date :

Apr 20, 2024

Anticipated Study Completion Date :

Dec 6, 2024

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Part 1: Cohort 1 INCAGN01876 every 2 weeks (Q2W) with retifanlimab every 4 weeks (Q4W).	Biological: INCAGN01876 INCAGN1876 will be adminstered via IV at at the protocol-defined dose and schedule according to cohort and treatment group enrollment. Biological: retifanlimab retifanlimab will be administered via IV Q4W
Experimental: Part 1: Cohort 2 INCAGN01876 Q2W with retifanlimab Q4W.	Biological: INCAGN01876 INCAGN1876 will be adminstered via IV at at the protocol-defined dose and schedule according to cohort and treatment group enrollment. Biological: retifanlimab retifanlimab will be administered via IV Q4W
Experimental: Part 2 (Expansion): Treatment Group A INCAGN01876 and retifanlimab combination in participants who have been previously treated with anti-PD-(L)1 therapy.	Biological: INCAGN01876 INCAGN1876 will be adminstered via IV at at the protocol-defined dose and schedule according to cohort and treatment group enrollment. Biological: retifanlimab retifanlimab will be administered via IV Q4W
Experimental: Part 2 (Expansion): Treatment Group B INCAGN01876 and retifanlimab combination in participants who are naive to anti-PD-(L)1 therapy.	Biological: INCAGN01876 INCAGN1876 will be adminstered via IV at at the protocol-defined dose and schedule according to cohort and treatment group enrollment. Biological: retifanlimab retifanlimab will be administered via IV Q4W

Outcome Measures

Primary Outcome Measures

Part 1: Participants With Treatment-Emergent Adverse Events (TEAEs) [Screening through 90 days after end of treatment, up to 24 months]
A TEAE is any adverse event (AE) either reported for the first time or worsening of a pre-existing event after the first dose of study treatment.
Objective response rate (ORR) based on Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 [Assessed every 8 weeks for 12 months, thereafter every 12 weeks up to the end of treatment, up to 24 months.]
Defined as the percentage of participants having complete response (CR) or partial response (PR).

Secondary Outcome Measures

Duration of response (DOR) based on RECIST v1.1 and mRECIST [Assessed every 8 weeks for 12 months, then every 12 weeks, up to 24 months.]
Defined as the time from the earliest date of disease response (CR or PR) until earliest date of disease progression or death due to any cause.
Disease control rate (DCR) based on RECIST v1.1 and mRECIST [Assessed every 8 weeks for 12 months, then every 12 weeks, up to 24 months.]
Defined as the percentage of participants having CR, PR, or stable disease (SD).
Progression-free survival (PFS) based on RECIST v1.1 and mRECIST [Assessed every 8 weeks for 12 months, then every 12 weeks, up to 24 months.]
Defined as the time from the start of combination therapy until the earliest date of disease progression or death due to any cause.
Part 2: Participants With Treatment-Emergent Adverse Events (TEAEs) [Screening through 90 days after end of treatment, up to 24 months]
A TEAE is any adverse event (AE) either reported for the first time or worsening of a pre-existing event after the first dose of study treatment.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 99 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Histologically or cytologically confirmed recurrent or metastatic HNSCC (oral cavity, oropharynx, hypopharynx, or larynx), that is not amenable to local therapy with curative intent (surgery or radiation therapy with or without chemotherapy). Participants with squamous cell carcinomas of the nasopharynx, salivary gland, or nonsquamous cell histology are excluded.
Documented progression on or after PD-(L)1 inhibitor alone or in combination with platinum-based chemotherapy for recurrent or metastatic HNSCC. Exception: Treatment Group B (Part 2, expansion): PD-(L)1-naïve.
ECOG performance status of 0 to 1.
Measurable disease based on RECIST v1.1.
Mandatory pre-treatment and on-treatment tumor biopsies.
GITR-positive tumor confirmed by central laboratory before study treatment start.
Willingness to avoid pregnancy or fathering children.

Exclusion Criteria:

Have received chemotherapy, targeted small molecule therapy or curative radiation within 21 days of first dose of study drug; prior mAB for anticancer therapy other within 28 days of first dose of study drug; or investigational study drugs or devices within 28 days or five half-lives prior to enrollment unless approved by medical monitor.
Prior treatment with any TNF Super Family agonist therapy.
Have not recovered to ≤ Grade 1 from toxic effects of prior therapy.
Laboratory and medical history parameters not within the Protocol-defined range before the first administration of study treatment.

Known active HBV or HCV, or Known to be seropositive for HIV.

Have an active autoimmune disease that has required systemic treatment in past 2 years (i.e., with use of disease modifying agents, corticosteroids, or immunosuppressive drugs).
Have an active autoimmune disease that has required systemic treatment in past 2 years (i.e., with use of disease modifying agents, corticosteroids, or immunosuppressive drugs).
Known active infections requiring systemic treatment.