← Back to Search

HIF-2alpha Inhibitor

PT2385 for Renal Cell Carcinoma

Phase 2
Waitlist Available
Research Sponsored by Peloton Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
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 4-5 years
Awards & highlights

Study Summary

This trial will study the effects of PT2385 on VHL-associated ccRCC tumors. The primary goal is to measure the overall response rate.

Eligible Conditions
  • Von Hippel-Lindau Syndrome
  • Von Hippel-Lindau Disease
  • Renal Cell Carcinoma

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4-5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 4-5 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Overall Response Rate (ORR)
Secondary outcome measures
Duration of Response (DOR)
Number of Participants who Discontinue Study Intervention Due to an AE.
Number of Participants who Experience One or More Adverse Events (AEs)
+2 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: PT2385 TabletsExperimental Treatment1 Intervention
Twenty-five patients will be enrolled in each stage of a two-stage design
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
PT2385 Tablets
2017
Completed Phase 2
~10

Find a Location

Who is running the clinical trial?

National Institutes of Health (NIH)NIH
2,696 Previous Clinical Trials
6,952,575 Total Patients Enrolled
Peloton Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)Lead Sponsor
7 Previous Clinical Trials
454 Total Patients Enrolled
Peloton Therapeutics, Inc.Lead Sponsor
7 Previous Clinical Trials
454 Total Patients Enrolled

Media Library

PT2385 Tablets (HIF-2alpha Inhibitor) Clinical Trial Eligibility Overview. Trial Name: NCT03108066 — Phase 2
PT2385 Tablets (HIF-2alpha Inhibitor) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03108066 — Phase 2
Von Hippel-Lindau Syndrome Research Study Groups: PT2385 Tablets
Von Hippel-Lindau Syndrome Clinical Trial 2023: PT2385 Tablets Highlights & Side Effects. Trial Name: NCT03108066 — Phase 2

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many people are participating in this clinical experiment?

"At this time, enrolment for the trial is temporarily closed. The posting date was April 24th 2017 and it was last modified on August 10th 2022. If you're looking to join a study, 3966 studies are currently accepting patients with von hippel-lindau disease while 3 trials are recruiting participants to test PT2385 Tablets."

Answered by AI

Is this experimental trial a pioneering endeavor?

"Peloton Therapeutics, Inc. first initiated research on PT2385 Tablets in 2014 and the drug was granted Phase 1 approval following a study involving 110 patients. Presently, 3 studies of this medication are underway across 22 cities within one nation."

Answered by AI

Is this study currently enlisting participants?

"Records on clinicaltrials.gov demonstrate that this trial has ceased recruitment, as the last update was made in August of 2022 and it launched back in April 2017. Despite no longer accepting participants, there are currently 3969 other trials recruiting patients worldwide."

Answered by AI

Has the FDA granted clearance to PT2385 Tablets?

"Leveraging our proprietary safety assessment scale, PT2385 Tablets have been tentatively granted a score of 2. This is because there has only been limited evidence that attests to their security and none yet indicating efficacy."

Answered by AI

Are there any documented precedents of PT2385 Tablets being tested in clinical trials?

"Presently, there are three ongoing trials for PT2385 Tablets and none have reached Phase 3. Trials taking place in Bethesda, Maryland serve as the epicentre of these investigations, though 27 other sites throughout America are also running studies on this medication."

Answered by AI
~1 spots leftby Apr 2025