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CR6086/AGEN2034 Combination in Stage IV pMMR - MSS CRC, and Other Metastatic GI Cancers

Phase 1
Recruiting
Conditions
Metastatic Microsatellite-stable Colorectal Cancer
Gastric Cancer
Solid Tumor
Refractory Metastatic Colorectal Cancer
Mismatch Repair Protein Proficient
Metastatic GI Cancers
Interventions
Biological: AGEN2034
Registration Number
NCT05205330
Lead Sponsor
Rottapharm Biotech
Brief Summary

This Phase Ib/IIa study comprises a Main Study and a Study Extension.

The Main Study has been designed according to a 3+3 dose escalation/dose expansion design in MSS mCRC patients. A dose expansion will be conducted at both the intermediate and high dose levels, if tolerated, with the purpose of generating additional and more robust safety and preliminary efficacy data.

The Study Extension explores in other metastatic GI cancers the CR6086 recommended dose for expansion (RDE) obtained in the Main Study.

No control arm was included, as the target patient population of this study consists of patients in whom the overall survival is less than 6 months and treatment options are very limited and often poorly tolerated, making unlikely that the study results can be significantly biased.

Detailed Description

In this study, the combination of the PGE2 inhibition (through the EP4 receptor antagonist CR6086) with the immune checkpoint blockade (through the anti-PD-1 AGEN2034) is being evaluated in pMMR-MSS mCRC and other metastatic GI cancers. CR6086 (vorbipiprant) is a potent and selective, orally bioavailable, targeted immunomodulator small molecule acting as an EP4 receptor antagonist. AGEN2034 (balstilimab) is a novel, fully human monoclonal immunoglobulin G4 antibody, designed to block programmed cell death 1 (PD-1) from interacting with its ligands (PD-L) PD-L1 and PD-L2, currently being developed for the treatment of advanced malignancies. EP4 receptor antagonists turn the status of the tumor microenvironment into a favourable one, i.e. immune-responsive, representing thus a rational therapeutic approach in combination with ICIs in primarily refractory cancers.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
55
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
other mGI cancersCR608614-day cycles of combined AGEN2034 3 mg/Kg iv on D1 of each cycle, and oral CR6086 90 mg twice a day for 14 days
30 mg (Dose Level 1)AGEN203414-day cycles of combined AGEN2034 3 mg/Kg iv on D1 of each cycle, and oral CR6086 30 mg twice a day for 14 days
90 mg (Dose Level 2)AGEN203414-day cycles of combined AGEN2034 3 mg/Kg iv on D1 of each cycle, and oral CR6086 90 mg twice a day for 14 days
180 mg (Dose Level 3)AGEN203414-day cycles of combined AGEN2034 3 mg/Kg iv on D1 of each cycle, and oral CR6086 180 mg twice a day for 14 days
other mGI cancersAGEN203414-day cycles of combined AGEN2034 3 mg/Kg iv on D1 of each cycle, and oral CR6086 90 mg twice a day for 14 days
180 mg (Dose Level 3)CR608614-day cycles of combined AGEN2034 3 mg/Kg iv on D1 of each cycle, and oral CR6086 180 mg twice a day for 14 days
30 mg (Dose Level 1)CR608614-day cycles of combined AGEN2034 3 mg/Kg iv on D1 of each cycle, and oral CR6086 30 mg twice a day for 14 days
90 mg (Dose Level 2)CR608614-day cycles of combined AGEN2034 3 mg/Kg iv on D1 of each cycle, and oral CR6086 90 mg twice a day for 14 days
Primary Outcome Measures
NameTimeMethod
Safety and Tolerability of CR6086 combined with AGEN2034From the time of the first dose up to 24 weeks of treatment

Incidence of TEAEs using NCI CTCAE v5.0

Disease Control rate (DCR)up to 24 weeks of treatment

Proportion of patients who have achieved CR, PR, or stable disease (SD) per RECIST 1.1 / iRECIST

Secondary Outcome Measures
NameTimeMethod
Progression-Free Survival Rate (PFSR)throughout the study, up to 2 years

Proportion of patients alive and free of disease progression per RECIST 1.1 / iRECIST at specific timepoints, or death by any cause in the absence of progression

Overall Survival (OS)throughout the study, up to 2 years

Time from the first dose of study drugs to the date of death by any cause

Duration Of Response (DOR)throughout the study, up to 2 years

Time from first documentation of response (CR or PR) until the time of first documentation of disease progression per RECIST 1.1 / iRECIST

Progression-Free Survival (PFR)throughout the study, up to 2 years

Time from the first dose of study drugs to the earlier date of assessment of progression per RECIST 1.1 / iRECIST, or death by any cause in the absence of progression

Objective Response Rate (ORR)throughout the study, up to 2 years

Proportion of patients who have achieved CR or PR per RECIST 1.1 / iRECIST

Safety and Tolerability of CR6086 combined with AGEN2034throughout the study, up to 2 years

Incidence of TEAEs

Trial Locations

Locations (1)

Istituto Nazionale dei Tumori

🇮🇹

Milano, MI, Italy

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