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Completed Phase 1Phase 2 Interventional Results available

A Study of Etigilimab and Nivolumab in Participants With Locally Advanced or Metastatic Tumors

ClinicalTrials.gov ID: NCT04761198

Public ClinicalTrials.gov record NCT04761198. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 2:24 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b/2 Open-Label Study of the Efficacy and Safety of Etigilimab (MPH313) Administered in Combination With Nivolumab to Subjects With Locally Advanced or Metastatic Solid Tumors (ACTIVATE)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is an open-label, phase 1b/2, multicenter study designed to evaluate the efficacy, safety, tolerability, pharmacokinetics (PK), and pharmacodynamics of etigilimab in combination with nivolumab in participants with locally advanced or metastatic solid tumors. Participants will be assigned to receive etigilimab (every 2 weeks) in combination with nivolumab (240 milligrams \[mg\] every 2 weeks).

Study identification

NCT ID
NCT04761198
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Mereo BioPharma
Industry
Enrollment
76 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 23, 2021 (Actual)
Primary completion
Oct 30, 2023 (Actual)
Completion
Oct 30, 2023 (Actual)
Last update posted
Mar 17, 2025

2021 – 2023

United States locations

U.S. sites
14
U.S. states
13
U.S. cities
14
Facility City State ZIP Site status
Mereo Investigator Site Phoenix Arizona 85054 —
Mereo Investigator Site Greenbrae California 94904 —
Mereo Investigator Site Los Angeles California 90025 —
Mereo Investigator Site Jacksonville Florida 32224 —
Mereo Investigator Site Boston Massachusetts 02215 —
Mereo Investigator Site Ann Arbor Michigan 48109 —
Mereo Investigator Site Rochester Minnesota 55905 —
Mereo Investigator Site New York New York 10065 —
Mereo Investigator Site Durham North Carolina 27710 —
Mereo Investigator Site Oklahoma City Oklahoma 73104 —
Mereo Investigator Site Nashville Tennessee 37203 —
Mereo Investigator Site Houston Texas 77030 —
Mereo Investigator Site West Valley City Utah 84119 —
Mereo Investigator Site Fairfax Virginia 22031 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04761198, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 17, 2025 · Synced Oct 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04761198 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →