A Phase 1 Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety and Tolerability of Single and Multiple Ascending Doses of VIB9600 by Intravenous Infusion or Subcutaneous Injection in Healthy Subjects
A Phase 1 Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety and Tolerability of Single and Multiple Ascending Doses of VIB9600 by Intravenous Infusion or Subcutaneous Injection in Healthy Subjects
Overall design: Single-center, randomized, blinded, placebo-controlled single- and multiple-ascending dose study in healthy adult subjects.
This first-time-in-human (FTIH) SAD and MAD studies in healthy adult subjects will be conducted at one site in the United States of America (USA) on IV and SC VIB9600.
Study acquired from Horizon in 2024. Originally Viela Bio was the sponsor.
Key Inclusion Criteria:
Key Exclusion Criteria:
Concurrent enrollment in another clinical study involving an investigational treatment.
Received administration of an investigational drug or participated in a device trial within 3 months prior to screening (Visit 1).
Subject is a participating investigator, sub-investigator, study coordinator, or employee of the participating site, or is a first-degree relative of the aforementioned.
History, or a reason to believe that a subject has a history, of drug or alcohol abuse within the 2 years prior to screening.
Positive test for drugs of abuse.
Donation of blood or blood products in excess of 500 mL within 3 months prior to screening. Not agreeing to refrain from blood or blood product donations during study participation.
Receiving any of the prohibited concomitant medications: