Skip to main content
OpenTrials
Completed

NCT Number: NCT06425861

A First in Human Trial Evaluating THB335 in Healthy Participants

This study is a double blind, randomized, placebo-controlled, Phase 1 study in three parts: single ascending doses and food effect (Part 1), multiple ascending doses (Part 2) and Relative Bioavailability of Two Formulations (Part 3).

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

QPS Miami

Miami, Florida, 33143, United States

About this study

THB335 is a highly potent and selective inhibitor of the receptor tyrosine kinase KIT that is expressed on mast cells.

The study will evaluate the safety, pharmacokinetics, pharmacodynamics, and food effect profile of THB335 administered orally in healthy participants.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • In good health, determined by no clinically significant findings from medical history, 12 lead electrocardiogram (ECG), vital sign measurements, and clinical laboratory evaluations
  • Males or females, of any race, between 18 and 65 years of age, inclusive.
  • Participants must understand the nature of the study and must provide signed and dated written informed consent in accordance with local regulations before the conduct of any study related procedures
  • Body weight of ≥ 50.0 kg for men and ≥ 45.0 kg for women and Body Mass Index (BMI) of 17.5-32.0 kg/m2 (inclusive) at Screening

Exclusion criteria

  • Significant history or clinical manifestation of cancer or any metabolic, allergic, dermatological, hepatic, biliary, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, respiratory, endocrine, or psychiatric disorder
  • Vaccinated within 14 days prior to Day -1 or intention to receive vaccination during the study
  • A positive urine drug screen/alcohol breath test
  • The participant currently smokes, vapes, or uses nicotine-containing products.

Treatment and study plan

THB335 single dose

Drug

Single dose as oral capsule

Single Dose Placebo

Drug

Single dose as oral capsule

THB335 fasted/fed

Drug

Single dose fasted and fed as oral capsule

Placebo fasted/fed

Drug

Single dose fasted and fed as oral capsule

THB335 multiple dose

Drug

Multiple ascending doses oral capsule

Multiple dose placebo

Drug

Multiple doses oral capsule

Primary outcomes

  1. Number of Participants with Treatment-Related Adverse Events

    Time frame: Part 1 Day 1 through Day 9 (end of study), and Part 2 Day 1 through Day 29 (end of study)

Secondary outcomes

  1. Maximum observed plasma concentration (Cmax)

    Time frame: Part 1, and Part 2 on Day 1. Part 2 on Day 14

  2. Time to Cmax (Tmax)

    Time frame: Part 1, and Part 2 on Day 1. Part 2 on Day 14

  3. Area under the plasma concentration-time curve (AUC)

    Time frame: Part 1, and Part 2 on Day 1. Part 2 on Day 14

Sponsors and collaborators

Lead sponsor

Third Harmonic Bio, Inc.

Industry

Registry information

Official study title

A Randomized, Double-Blind, Placebo-Controlled, Phase 1, Single and Multiple Ascending Dose Study to Assess the Safety, Pharmacokinetics, Pharmacodynamics, and Food Effect of THB335 in Healthy Participants

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
May 22, 2024
Registry last updated
Dec 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.