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Clinical Trials associated with REGN-6490A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study of the Safety, Tolerability and Pharmacokinetics of REGN6490 in Healthy Volunteers
The primary objective of the study is to evaluate the safety and tolerability of single ascending intravenous (IV) and subcutaneous (SC) doses of REGN6490 in healthy adult participants
The secondary objectives of the study are to:
Characterize the pharmacokinetic (PK) profile of single IV and SC doses of REGN6490 in healthy adult participants
Assess immunogenicity of REGN6490 in healthy adult participants dosed with a single IV or SC dose of REGN6490
A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of REGN6490 in Healthy Japanese Volunteers
The primary objective of the study is to evaluate the safety and tolerability of 3 single ascending subcutaneous (SC) doses and 1 single intravenous (IV) dose of REGN6490 in healthy first-generation Japanese adult participants
The secondary objectives of the study are:
To characterize the pharmacokinetic (PK) profile of single SC and IV doses of REGN6490 in healthy first-generation Japanese adult participants
Assess immunogenicity of REGN6490 in healthy first-generation Japanese adult participants dosed with a single IV or SC dose of REGN6490
100 Clinical Results associated with REGN-6490
100 Translational Medicine associated with REGN-6490
100 Patents (Medical) associated with REGN-6490
100 Deals associated with REGN-6490