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Phase I Study of ICP-332 in Healthy Subjects

I

InnoCare Pharma

Status and phase

Enrolling
Phase 1

Conditions

Healthy Subjects

Treatments

Drug: ICP-332 Tablets
Drug: ICP-332 Placebo Tablets

Study type

Interventional

Funder types

Industry

Identifiers

NCT06530966
ICP-CL-00605

Details and patient eligibility

About

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

Enrollment

24 estimated patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

24 participants in 2 patient groups, including a placebo group

ICP-332
Experimental group
Treatment:
Drug: ICP-332 Tablets
Placebo
Placebo Comparator group
Treatment:
Drug: ICP-332 Placebo Tablets

Trial contacts and locations

1

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Central trial contact

Alexia Lu

Data sourced from clinicaltrials.gov

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