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A Phase 1/2, Open-Label, Single and Multiple Ascending Dose Study of CRMA-1001 in Adults With Chronic Hepatitis B

Plain-language summary

This study evaluates the drug CRMA-1001 and its different doses in adults with chronic hepatitis B. Adults aged 18 to 64, weighing 45 to 150 kg, who have chronic hepatitis B and are on oral antiviral therapy may take part. The study is in Phase 1/Phase 2 and is currently recruiting participants.

The summary above is a plain-language rendering of the official record. The original English title is shown for reference.

Trial details

Phase
PHASE1/PHASE2
Status
Recruiting
Sponsor
nChroma Bio
Intervention
CRMA-1001
Start date
12/22/2025
Estimated completion
12/31/2032
Countries
France, Hong Kong, New Zealand, United Kingdom

Related genes

Locations

  • Lyon, France
  • Hong Kong, Hong Kong
  • Auckland, New Zealand
  • London, United Kingdom

Eligibility criteria

Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.

Inclusion Criteria:

* Male/Female, weight 45-150 kg, age 18-64, inclusive
* Diagnosed with Chronic Hepatitis B
* On oral antiviral therapy
* ALT and AST \<= 1.5 x ULN
* Total bilirubin \<= ULN

Exclusion Criteria:

* Significant hepatic fibrosis or cirrhosis
* Current or prior liver disease other than HBV
* Other protocol-defined inclusion/exclusion criteria may apply
This is not medical advice. Consult your specialist.
View the official record on ClinicalTrials.gov →