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NCT05147272 · ClinicalTrials.gov registry record · Phase 1

Study of RP-6306 With Gemcitabine in Advanced Solid Tumors

A Phase 1 study, sponsored by Debiopharm International.

Terminated
Registry status
Phase 1
Development phase
67
Enrollment target

NCT05147272 is a Phase 1 study that was terminated before completion, run by Debiopharm International. The registered enrollment target is 67 participants.

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The verdict

NCT05147272, a Phase 1 study, was terminated before completion, sponsored by Debiopharm International.

TERMINATED
Registry status
Phase 1
Development phase
67 participants
Enrollment target

Study Summary

The primary purpose of this study is to assess the safety and tolerability of RP-6306 in combination gemcitabine, in patients with eligible advanced solid tumors, determine the maximum tolerated dose (MTD) of RP-6306 in combination with gemcitabine, identify a recommended phase 2 dose (RP2D) and preferred schedule, examine preliminary pharmacokinetics (PK) and assess anti-tumor activity.

Interventions

  • DRUG RP-6306 (oral PKMYT1 inhibitor)

Trial Details

FieldValue
Enrollment Target 67 participants
Start Date 2021-12-16
Est. Completion 2024-08-28
Phase Phase 1

Sponsor

Debiopharm International

30 total trials

What the Registry Record Tells You About NCT05147272

The ClinicalTrials.gov registry entry for NCT05147272 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 67 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Debiopharm International, which has 30 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which RP-6306 (oral PKMYT1 inhibitor) is the first listed.

NCT05147272 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05147272 about?

NCT05147272 is a clinical study titled "Study of RP-6306 With Gemcitabine in Advanced Solid Tumors". The primary purpose of this study is to assess the safety and tolerability of RP-6306 in combination gemcitabine, in patients with eligible advanced solid tumors, determine the maximum tolerated dose (MTD) of RP-6306 in combination with gemcitabine, identify a recommended phase 2 dose (RP2D) and pre...

What is the current status of trial NCT05147272?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 67 participants. The study started on 2021-12-16. Estimated completion is 2024-08-28.

What interventions are being tested in trial NCT05147272?

The interventions under investigation include: RP-6306 (oral PKMYT1 inhibitor) (DRUG).

Who is sponsoring clinical trial NCT05147272?

This trial is sponsored by Debiopharm International, which has 30 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.