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NCT02829723 · ClinicalTrials.gov registry record · Phase 1

A Study of BLZ945 Single Agent or BLZ945 in Combination With PDR001 in Advanced Solid Tumors

A Phase 1 study, sponsored by Novartis Pharmaceuticals.

Terminated
Registry status
Phase 1
Development phase
192
Enrollment target

NCT02829723: Clinical Trial Phase 1 study, sponsored by Novartis Pharmaceuticals.

NCT02829723 is a Phase 1 study that was terminated before completion, run by Novartis Pharmaceuticals. The registered enrollment target is 192 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (220% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02829723, a Phase 1 study, was terminated before completion, sponsored by Novartis Pharmaceuticals.

TERMINATED
Registry status
Phase 1
Development phase
192 participants
Enrollment target

Study Summary

The purpose of this first-in-human (FIH) study of BLZ945 given as a single agent or in combination with PDR001 was to characterize the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and anti-tumor activity of BLZ945, administered orally, as a single agent or in combination with PDR001, administered intravenously (i.v.) in adult patients with advanced solid tumors.

Primary Outcome

Number of participants with AEs (any AE regardless of seriousness) and SAEs, including changes from baseline in vital signs, electrocardiograms and laboratory results qualifying and reported as AEs. The on-treatment period is defined from the day of first administration of study treatment up to 30 days after the date of its last administration.

Interventions

  • DRUG PDR001
  • DRUG BLZ945

Trial Details

FieldValue
Enrollment Target 192 participants
Start Date 2016-10-21
Est. Completion 2022-12-01
Phase Phase 1
Novartis Pharmaceuticals

1,375 total trials

Why NCT02829723 stopped before completion

NCT02829723 is an interventional study that assigns participants to a tested intervention. The registered 192 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 (220% higher).

The record links to 0 conditions, and to 2 interventions - of which PDR001 is the first listed.

NCT02829723 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02829723 about?

NCT02829723 is a clinical study titled "A Study of BLZ945 Single Agent or BLZ945 in Combination With PDR001 in Advanced Solid Tumors". The purpose of this first-in-human (FIH) study of BLZ945 given as a single agent or in combination with PDR001 was to characterize the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and anti-tumor activity of BLZ945, administered orally, as a single agent or in combination with PDR00...

What is the current status of trial NCT02829723?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 192 participants. The study started on 2016-10-21. Estimated completion is 2022-12-01.

What interventions are being tested in trial NCT02829723?

The interventions under investigation include: PDR001 (DRUG), BLZ945 (DRUG).

Who is sponsoring clinical trial NCT02829723?

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

How this trial's enrollment target compares

Where NCT02829723's enrollment target sits among peer trials

192 282nd of 2000 higher than 1,718 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 NCT02829723, the US trial registry maintained by the National Library of Medicine. NCT02829723 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.