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Completed Phase 1Phase 2 Interventional Results available

Safety and Efficacy of Tenalisib (RP6530) in Combination With Romidepsin in Patients With Relapsed/Refractory T-cell Lymphoma

ClinicalTrials.gov ID: NCT03770000

Public ClinicalTrials.gov record NCT03770000. 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 21, 2026, 12:52 AM EDT

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

Official title

An Open Label, Phase I/II Study to Evaluate the Safety and Efficacy of Tenalisib (RP6530), a Novel PI3K δ/γ Dual Inhibitor Given in Combination With a Histone Deacetylase (HDAC) Inhibitor, Romidepsin in Adult Patients With Relapsed/Refractory T-cell Lymphoma

Brief summary

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

To characterize safety, tolerability and to establish the maximum tolerated dose (MTD) of Tenalisib in combination with Romidepsin in patients with R/R T-cell lymphoma.

Study identification

NCT ID
NCT03770000
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Rhizen Pharmaceuticals SA
Industry
Enrollment
33 participants

Conditions and interventions

Interventions

Drug

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 12, 2019 (Actual)
Primary completion
May 14, 2021 (Actual)
Completion
May 14, 2021 (Actual)
Last update posted
Oct 28, 2022

2019 – 2021

United States locations

U.S. sites
15
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
USC/Norris Comprehensive Cancer Center Los Angeles California 90033 —
University of California, Hellen Diller Family Comprehensive Cancer Center San Francisco California 94143 —
University of Colorado Cancer Center Aurora Colorado 80045 —
University of Miami-Sylvester Comprehensive Cancer Center Miami Florida 33136 —
Winship Cancer Institute of Emory University Atlanta Georgia 30322 —
Rush University Cancer Center Chicago Illinois 60612 —
The University of Kansas Cancer Center Fairway Kansas 66205 —
Norton Cancer Institute, St Matthews Campus Louisville Kentucky 40207 —
University of Michigan Ann Arbor Michigan 48109 —
John Theurer Cancer Center, Hackensack University Medical Center Hackensack New Jersey 07601 —
Roswell Park Comprehensive Cancer Center Buffalo New York 14263 —
Cleveland Clinic Taussig Cancer Institute Cleveland Ohio 44195 —
Oregon Health & Science University Portland Oregon 97239 —
Vanderbilt Ingram Cancer Center Nashville Tennessee 37232-5505 —
The University of Texas MD Anderson Cancer Center, Houston Texas 77030 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03770000, 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, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03770000 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →