Study of VE800 and Nivolumab in Patients With Selected Types of Advanced or Metastatic Cancer (ConsortiumIO)

Vedanta Biosciences

Status and phase

Completed

Phase 2

Phase 1

Conditions

Metastatic Cancer

Melanoma

Gastric Cancer

Gastroesophageal Junction Adenocarcinoma

Colorectal Cancer

Treatments

Biological: VE800

Drug: Nivolumab

Drug: Vancomycin Oral Capsule

Study type

Interventional

Funder types

Industry

Identifiers

NCT04208958

VE800-001

Details and patient eligibility

About

This study evaluated the safety and efficacy of VE800 in combination with nivolumab in patients with selected types of advanced or metastatic cancer

Full description

CONSORTIUM-IO was the first-in-human multicenter, open-label study; the main objectives were to evaluate:

Safety and tolerability of VE800 in combination with nivolumab
Efficacy as measured by objective response rate

The study planned to enroll approximately 111 patients with melanoma, gastric/gastroesophageal junction (GEJ) adenocarcinoma, or microsatellite-stable (MSS) colorectal cancer (CRC).

Nivolumab is already approved by the U.S. Food and Drug Administration (FDA), however, it is not approved for the study cancer indications. VE800 was the investigational product, which was designed to enhance the immune response to the tumor.

Enrollment

56 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Partial Inclusion Criteria:

Patients with advanced or metastatic cancer who had received no more than 3 lines of prior systemic therapy for advanced/metastatic disease.
Histologically diagnosed advanced (unresectable) or metastatic cancer with at least one measurable lesion as per RECIST 1.1
Tumor lesions amenable for biopsy, if deemed safe by the investigator
Toxicity from prior cancer therapy should have resolved to Common Terminology Criteria for Adverse Events (CTCAE) Grade ≤ 1 (excluding alopecia and neuropathy, where up to Grade 2 residual was allowed)

Partial Exclusion Criteria:

Prior treatment with immune checkpoint inhibitor (iCPI) (Note: this criterion did not apply to patients with melanoma)
Receipt of any conventional or investigational systemic anti-cancer therapy within 21 days prior to the first dose of vancomycin
Concurrent chemotherapy, immunotherapy, biologic, or hormonal anti-cancer therapy. Agents such as bisphosphonates or denosumab were acceptable as prophylaxis for bone metastasis.
Patients must not have received a transfusion (platelets or red blood cells) within 4 weeks of the first dose of study treatment
Patients with an active, known or suspected autoimmune disease. Patients with type I diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders (such as vitiligo, psoriasis, or alopecia) not requiring systemic treatment were permitted to enroll.
Patients with known active hepatitis (e.g., hepatitis B or C) NOTE: Patients with previously treated hepatitis B or C were permitted to enroll if there was evidence of documented resolution of infection.
Received a fecal transplant, spore or other preparation of fecal material, isolated bacterial products, genetically modified bacteria, or VE800