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NCT02890069 · ClinicalTrials.gov registry record · Phase 1

A Study of PDR001 in Combination With LCL161, Everolimus or Panobinostat

A Phase 1 study of Colorectal Cancer, Non-small Cell Lung Carcinoma (Adenocarcinoma), Triple Negative Breast Cancer, Renal Cell Carcinoma, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
298
Enrollment target
20
Study locations

NCT02890069: Completed Phase 1 study of Colorectal Cancer, Non-small Cell Lung Carcinoma (Adenocarcinoma), Triple Negative Breast Cancer, Renal Cell Carcinoma, sponsored by Novartis Pharmaceuticals.

NCT02890069 is a Phase 1 study of Colorectal Cancer, Non-small Cell Lung Carcinoma (Adenocarcinoma), Triple Negative Breast Cancer, Renal Cell Carcinoma that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 298 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (397% higher). The trial reports 20 study locations across 12 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02890069, a Phase 1 study of Colorectal Cancer, Non-small Cell Lung Carcinoma (Adenocarcinoma), Triple Negative Breast Cancer, Renal Cell Carcinoma, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
298 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this study was to combine the PDR001 checkpoint inhibitor with several agents with immunomodulatory activity to identify the doses and schedule for combination therapy and to preliminarily assess the safety, tolerability, pharmacological and clinical activity of these combinations.

Primary Outcome

During the first two cycles Cycle = 28 days

Interventions

  • DRUG Everolimus
  • DRUG Panobinostat
  • BIOLOGICAL PDR001
  • DRUG LCL161
  • DRUG QBM076

Study Locations (20)

Other

  • Novartis Investigative Site - Jena
  • Novartis Investigative Site - Ulm
  • Novartis Investigative Site - Würzburg
  • Novartis Investigative Site - Amsterdam
  • Novartis Investigative Site - Leiden
  • Novartis Investigative Site - Rotterdam
  • Novartis Investigative Site - Utrecht
  • Novartis Investigative Site - Seoul

Texas

  • University of Texas MD Anderson Cancer Center - Houston
  • UT Health San Antonio Mays Cancer Center - San Antonio

California

  • UCLA Santa Monica Hematology / Oncology SC - Santa Monica

Maryland

  • Sidney Kimmel Comprehensive Cancer Center - Baltimore

Massachusetts

  • Massachusetts General Hospital - Boston

Michigan

  • The Regents of the University of Michigan - Ann Arbor

Missouri

  • Washington University Medical School SC - St Louis

Utah

  • Huntsman Cancer Institute - Salt Lake City

Trial Details

FieldValue
Enrollment Target 298 participants
Start Date 2016-10-14
Est. Completion 2022-02-22
Phase Phase 1
Novartis Pharmaceuticals

1,375 total trials

What the finished NCT02890069 record still lists

NCT02890069 is an interventional study that assigns participants to a tested intervention. The registered 298 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (397% higher).

The record links to 1 condition, with Colorectal Cancer, Non-small Cell Lung Carcinoma (Adenocarcinoma), Triple Negative Breast Cancer, Renal Cell Carcinoma appearing as the primary indexed condition, and to 5 interventions - of which Everolimus is the first listed.

NCT02890069 names 20 study sites across 12 states, led by Other, Texas, California.

Frequently Asked Questions

What is clinical trial NCT02890069 about?

NCT02890069 is a clinical study titled "A Study of PDR001 in Combination With LCL161, Everolimus or Panobinostat". The purpose of this study was to combine the PDR001 checkpoint inhibitor with several agents with immunomodulatory activity to identify the doses and schedule for combination therapy and to preliminarily assess the safety, tolerability, pharmacological and clinical activity of these combinations.

What is the current status of trial NCT02890069?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 298 participants. The study started on 2016-10-14. Estimated completion is 2022-02-22.

What conditions does trial NCT02890069 study?

This clinical trial studies the following conditions: Colorectal Cancer, Non-small Cell Lung Carcinoma (Adenocarcinoma), Triple Negative Breast Cancer, Renal Cell Carcinoma.

What interventions are being tested in trial NCT02890069?

The interventions under investigation include: Everolimus (DRUG), Panobinostat (DRUG), PDR001 (BIOLOGICAL), LCL161 (DRUG), QBM076 (DRUG).

Who is sponsoring clinical trial NCT02890069?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02890069 being conducted?

This trial has 20 study locations across California, Maryland, Massachusetts, Michigan, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT02890069's enrollment target sits among peer trials

298 134th of 2000 higher than 1,866 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02890069, the US trial registry maintained by the National Library of Medicine. NCT02890069 (mid enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.