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Active, not recruiting Phase 1 Interventional

A Study of TSR-022 in Participants With Advanced Solid Tumors (AMBER)

ClinicalTrials.gov ID: NCT02817633

Public ClinicalTrials.gov record NCT02817633. 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 Nov 7, 2026, 5:21 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1 Dose Escalation and Cohort Expansion Study of TSR-022, an Anti-TIM-3 Monoclonal Antibody, in Patients With Advanced Solid Tumors (AMBER)

Brief summary

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

This is a first-in-human study evaluating the anti-T cell immunoglobulin and mucin containing protein-3 (TIM-3) antibody TSR-022. The study will be conducted in 2 parts with Part 1 consisting of dose escalation and Part 2 dose expansion. Part 1 will determine the recommended Phase 2 dose (RP2D) of TSR-022 and Part 2 will evaluate the antitumor activity of TSR-022 in combination with TSR-042 or docetaxel and as monotherapy.

Study identification

NCT ID
NCT02817633
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
Tesaro, Inc.
Industry
Enrollment
463 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
Jul 8, 2016 (Actual)
Primary completion
Mar 1, 2027 (Estimated)
Completion
Mar 1, 2027 (Estimated)
Last update posted
Oct 28, 2025

2016 – 2027

United States locations

U.S. sites
64
U.S. states
27
U.S. cities
59
Facility City State ZIP Site status
GSK Investigational Site Goodyear Arizona 85338 —
GSK Investigational Site Scottsdale Arizona 85258 —
GSK Investigational Site Tucson Arizona 85704 —
GSK Investigational Site Tucson Arizona 85711 —
GSK Investigational Site Encinitas California 92024 —
GSK Investigational Site Fountain Valley California 92708 —
GSK Investigational Site Los Angeles California 90024 —
GSK Investigational Site Los Angeles California 90025 —
GSK Investigational Site San Marcos California 92069 —
GSK Investigational Site Whittier California 90606 —
GSK Investigational Site Aurora Colorado 80012 —
GSK Investigational Site Aurora Colorado 80045 —
GSK Investigational Site Denver Colorado 80218 —
GSK Investigational Site New Haven Connecticut 06511 —
GSK Investigational Site Washington D.C. District of Columbia 20007 —
GSK Investigational Site Jacksonville Florida 32224 —
GSK Investigational Site Miami Florida 33140 —
GSK Investigational Site Sarasota Florida 34232 —
GSK Investigational Site Tampa Florida 33612 —
GSK Investigational Site Atlanta Georgia 30322 —
GSK Investigational Site Augusta Georgia 30912 —
GSK Investigational Site Arlington Heights Illinois 60005 —
GSK Investigational Site Chicago Illinois 60637 —
GSK Investigational Site Niles Illinois 60714 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Wichita Kansas 67214 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site Pikeville Kentucky 41501 —
GSK Investigational Site Wheaton Maryland 20850 —
GSK Investigational Site Boston Massachusetts 02114 —
GSK Investigational Site Detroit Michigan 48202 —
GSK Investigational Site Rochester Minnesota 55905 —
GSK Investigational Site Florissant Missouri 63031 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site St Louis Missouri 63129 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Hackensack New Jersey 07601 —
GSK Investigational Site New York New York 10016 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site Cincinnati Ohio 45242 —
GSK Investigational Site Cleveland Ohio 44106 —
GSK Investigational Site Toledo Ohio 43623 —
GSK Investigational Site Eugene Oregon 97401 —
GSK Investigational Site Vancouver Oregon 97213-2982 —
GSK Investigational Site Bethlehem Pennsylvania 18015 —
GSK Investigational Site Pittsburgh Pennsylvania 15232 —
GSK Investigational Site Charleston South Carolina 29425 —
GSK Investigational Site Greenville South Carolina 29605 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Longview Texas 75601 —
GSK Investigational Site McAllen Texas 78503-1298 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Temple Texas 76508 —
GSK Investigational Site Tyler Texas 75702 —
GSK Investigational Site Fairfax Virginia 22031 —
GSK Investigational Site Kennewick Washington 99336 —
GSK Investigational Site Puyallup Washington 98373 —
GSK Investigational Site Seattle Washington 98111 —
GSK Investigational Site Tacoma Washington 98405 —
GSK Investigational Site Madison Wisconsin 53792 —

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 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02817633, 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 Oct 28, 2025 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02817633 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →