Status:

COMPLETED

A Study to See How Safe and Tolerable Different Doses of REGN13335 Are When Administered Intravenously (IV) or Subcutaneously (SC) to Healthy Adult Participants

Lead Sponsor:

Regeneron Pharmaceuticals

Conditions:

Healthy Volunteers

Eligibility:

All Genders

18-55 years

Phase:

PHASE1

Brief Summary

This study is researching an experimental drug called REGN13335. This is the first time that REGN13335 will be given to people. This study will enroll healthy adults. The aim of the study is to see h...

Eligibility Criteria

Inclusion

  • Key
  • Has a body mass index between 18 and 32 kg/m\^2, inclusive, at the screening visit
  • Is judged by the investigator to be in good health based on medical history, physical examination, vital sign measurements, laboratory safety tests, and electrocardiograms (ECGs) performed prior to administration of study drug (ie, screening and baseline visit)
  • Key

Exclusion

  • 1\. History of clinically significant cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, psychiatric or neurological disease, as assessed by the investigator
  • NOTE: Other Protocol Defined Inclusion / Exclusion Criteria Apply.

Key Trial Info

Start Date :

December 6 2023

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 11 2025

Estimated Enrollment :

56 Patients enrolled

Trial Details

Trial ID

NCT06137482

Start Date

December 6 2023

End Date

February 11 2025

Last Update

March 19 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

New Zealand Clinical Research

Christchurch, Canterbury, New Zealand, 8011