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Pharmacokinetics and Tolerability of Trinbelimab in healthy volunteers

Phase 1
Registration Number
CTRI/2023/10/058310
Lead Sponsor
Bharat Serums and Vaccines Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Post-menopausal female subjects.

BMI between 18.5 and 29.9 kg/m2

Able to give voluntary written consent

Exclusion Criteria

Rh-D positive post menopausal female and who are positive for anti-D IgG antibodies

Positive test for pregnancy

History or presence of clinically significant disease

Known hypersensitivity to antiD immunoglobulin

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the PK parameters of single dose (300 mcg) of TrinbelimabTimepoint: Predose <br/ ><br>Post dose - 8 hours and 24 hours, then every day till day 10, every 2 weeks till day 113
Secondary Outcome Measures
NameTimeMethod
To assess the tolerability of TrinbelimabTimepoint: Throughout the study till the end of study AEs will be captured
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