RecruitingPhase 1NCT06530966

Phase I Study of ICP-332 in Healthy Subjects

A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Phase I Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ICP-332 in Healthy Subjects


Sponsor

InnoCare Pharma Inc.

Enrollment

24 participants

Start Date

Jul 23, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

A multiple ascending dose phase I study of ICP-332 in healthy subjects


Eligibility

Min Age: 18 YearsMax Age: 55 Years

Inclusion Criteria3

  • Voluntarily sign the informed consent form
  • Body mass index (BMI) of ≥ 18.5 kg/m2 and < 30 kg/m2
  • Male or infertile female subjects who are between 18-55 years old (inclusive)

Exclusion Criteria4

  • Significant current or past acute or chronic disease or condition.
  • A history of tuberculosis or current active/latent infection.
  • With a history of drug or food allergy, or allergy to any of the composition components of the study drug, or allergic disease.
  • Subjects with clinically significant abnormalities in the screening examinations.

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Interventions

DRUGICP-332 Tablets

Eligible patients will receive ICP-332 tablets orally as per the protocol

DRUGICP-332 Placebo Tablets

Eligible patients will receive ICP-332 placebo tablets orally as per the protocol


Locations(1)

Pharmaron CPC Inc.

Baltimore, Maryland, United States

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NCT06530966


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