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Checkpoint Inhibitor

Atezolizumab + Tiragolumab for Rare Cancers

Phase 2
Recruiting
Led By Jibran Ahmed
Research Sponsored by National Cancer Institute (NCI)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 2 years
Awards & highlights
No Placebo-Only Group

Summary

This trial tests if the combination of atezolizumab and tiragolumab can help treat patients with advanced rare solid tumors. Atezolizumab is a type of drug that helps the immune system fight cancer. These drugs aim to boost the immune system to fight cancer more effectively. The study will also collect samples to understand how the treatment works and who might benefit most from it.

Who is the study for?
Adults with advanced rare solid tumors that have progressed after standard therapy or lack a standard treatment. They must be willing to undergo biopsies, not qualify for higher priority trials, and have measurable disease. Key health criteria include stable organ function and controlled HIV or hepatitis if present. Pregnant women are excluded, and participants must agree to use contraception.
What is being tested?
The trial is testing the effectiveness of combining two immunotherapy drugs, Atezolizumab and Tiragolumab, in shrinking advanced stage rare solid tumors. It includes taking tissue samples before and after treatment to study the immune response against cancer.
What are the potential side effects?
Potential side effects may include reactions related to the immune system attacking normal cells leading to inflammation in various organs, infusion-related reactions similar to allergic responses during drug administration, fatigue, blood disorders like low counts of different types of blood cells which can increase infection risk.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 2 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 2 years for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Incidence of adverse events
Pharmacodynamic (PD) response rate
Secondary study objectives
Objective tumor response rate (ORR)

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Treatment (atezolizumab, tiragolumab)Experimental Treatment6 Interventions
Patients receive atezolizumab IV over 60 minutes and tiragolumab IV over 30-90 minutes on day 1 of each cycle. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients also undergo ECHO at baseline, undergo biopsy at baseline and on study, and undergo CT and collection of blood samples throughout the study.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Tiragolumab
2019
Completed Phase 3
~1390
Atezolizumab
2016
Completed Phase 3
~5860
Biopsy
2014
Completed Phase 4
~1090
Biospecimen Collection
2004
Completed Phase 3
~2020
Computed Tomography
2017
Completed Phase 2
~2740
Echocardiography
2013
Completed Phase 4
~11580

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Monoclonal antibodies like atezolizumab and tiragolumab enhance the immune system's ability to attack cancer cells by blocking inhibitory signals that tumors use to evade immune detection. Atezolizumab targets PD-L1, preventing it from binding to PD-1 on T cells, while tiragolumab targets TIGIT, another checkpoint protein. This dual blockade boosts T cell activity against tumors, potentially leading to more effective and durable responses. For solid tumor patients, these mechanisms offer hope for improved survival and tumor control by leveraging the body's own immune system to fight cancer.

Find a Location

Who is running the clinical trial?

National Cancer Institute (NCI)Lead Sponsor
13,917 Previous Clinical Trials
41,014,450 Total Patients Enrolled
Jibran AhmedPrincipal InvestigatorNational Cancer Institute LAO
Naoko TakebePrincipal InvestigatorNational Cancer Institute LAO
2 Previous Clinical Trials
95 Total Patients Enrolled

Media Library

Atezolizumab (Checkpoint Inhibitor) Clinical Trial Eligibility Overview. Trial Name: NCT05715281 — Phase 2
Solid Tumors Research Study Groups: Treatment (atezolizumab, tiragolumab)
Solid Tumors Clinical Trial 2023: Atezolizumab Highlights & Side Effects. Trial Name: NCT05715281 — Phase 2
Atezolizumab (Checkpoint Inhibitor) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05715281 — Phase 2
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