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ACTIVE NOT RECRUITING
NCT05781399
PHASE1/PHASE2

First-in-Human, Multiple Part Clinical Study of JNT-517 in Healthy Participants and in Participants With Phenylketonuria

Sponsor: Otsuka Pharmaceutical Development & Commercialization, Inc.

View on ClinicalTrials.gov

Summary

The goal of Parts A and B of this Phase 1/2, first-in-human, randomized study is to assess the safety, tolerability, and pharmacokinetics (PK) of single (SAD) and multiple (MAD) ascending doses of oral JNT-517 in healthy participants. In Part C, the goal is to evaluate the differences in bioavailability between a tablet and suspension formulation of JNT-517 and the food effect in healthy volunteers. All participants in Part C will receive JNT-517. The goal of Part D is to assess the safety, tolerability, PK, and effect on urinary Phe and other amino acids of JNT-517 in participants with phenylketonuria (PKU). Participants in Part D will receive either JNT-517 or placebo and will be blinded to their treatment assignment. The study consists of 6 parts: * Part A: SAD in healthy participants -randomized, double-blind, placebo-controlled * Part B: MAD in healthy participants (14 days)-randomized, double-blind, placebo-controlled * Part C: Relative bioavailability of 2 formulations and food effect in healthy participants-randomized, open-label * Part D: Phase 2 in participants with PKU (4 weeks)-randomized, double-blind, placebo-controlled * Part E: Phase 2 in participants with PKU (4 weeks) open label * Part F: SAD Phase 1 in healthy participants, randomized, double-blind, placebo-controlled In each part, participants will complete a Screening Period, a Treatment Period, and a Follow-up Period for safety.

Official title: A Phase 1/2, First-In-Human, Multiple Part, Single Ascending and Multiple Dose Study of JNT-517 in Healthy Participants and in Participants With Phenylketonuria

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

135

Start Date

2022-10-31

Completion Date

2025-12-15

Last Updated

2025-07-31

Healthy Volunteers

Yes

Conditions

Interventions

DRUG

JNT-517 Suspension

JNT-517 in on-site compounded suspension

DRUG

Placebo Suspension

On-site compounded placebo suspension

DRUG

JNT-517 Tablet

JNT-517 tablets, 25 mg and 75 mg

DRUG

Placebo Tablet

Matching film-coated placebo tablet

Locations (15)

University of Florida College of Medicine

Gainesville, Florida, United States

University of South Florida

Tampa, Florida, United States

Rare Disease Research

Atlanta, Georgia, United States

Ann & Robert H. Lurie Children's Hospital of Chicago

Chicago, Illinois, United States

University of Nebraska Medical Center

Omaha, Nebraska, United States

Oregon Health & Sciences University

Portland, Oregon, United States

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States

UPMC Children's Hospital of Pittsburgh

Pittsburgh, Pennsylvania, United States

UT Southwestern Medical Center

Dallas, Texas, United States

University of Texas Health Science Center at Houston

Houston, Texas, United States

Utah Health - The University of Utah Hospital

Salt Lake City, Utah, United States

Nucleus Network Melbourne

Melbourne, Melbourne VIC, Australia

Westmead Hospital

Westmead, New South Wales, Australia

Mater Misericordia Ltd

South Brisbane, Queensland, Australia

Royal Adelaide Hospital

Adelaide, South Australia, Australia