Phase II Study of Efficacy and Safety of HSK39297 Tablet in Treatment of Patients with Primary IgAN

NCT06670352 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2024-11-01

No results posted yet for this study

Summary

Evaluate the efficacy and safety of HSK39297 tablets in patients with primary IgAN

Conditions

  • IgA Nephropathy (IgAN)

Interventions

DRUG

Placebo

QD or BID, 24-weeks fixed dose.

DRUG

HSK39297 50mgBID

24-weeks fixed dose.

DRUG

HSK39297 100mgBID

24-weeks fixed dose.

DRUG

HSK39297 200mgQD

24-weeks fixed dose.

Sponsors & Collaborators

  • Haisco Pharmaceutical Group Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-12
Primary Completion
2025-11-23
Completion
2026-03-15

Countries

  • China

Study Locations

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Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06670352 on ClinicalTrials.gov