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A Phase 2b/3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of MK-1654 in Healthy Pre-Term and Full-Term Infants

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Privacy Notice: The data collected here will be used by UT Health San Antonio staff to contact you, either by email or by telephone, with the sole purpose of providing you with information regarding human study participation. You may be contacted in the future regarding studies similar to this one. Under no circumstances will we use your information for other purposes or share it with others. To the extent it is applicable, UT Health San Antonio complies with the General Data Protection Regulation (“GDPR”). Should you have any requests pertaining to your rights under the GDPR, please send it to: The IRB Reliance Team at irbreliance@uthscsa.edu | (210) 567-8555

Lay Description

Eligibility

Eligible Ages
Eligible Genders
Accepts Healthy Volunteers

Inclusion Criteria

Exclusion Criteria

Study Design

Arm Groups

Study Contact

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Diana Anzueto Guerra
210-567-5225
anzuetod@uthscsa.edu

Principal Investigator
Michael Odom

UT Health San Antonio

8403 Floyd Curl Dr
San Antonio, TX 78229

210-567-8555
IRBreliance@uthscsa.edu

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A Phase 2b/3 Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy and Safety of MK-1654 in Healthy Pre-Term and Full-Term Infants

Lay Description

Category

Eligibility

Inclusion Criteria

Exclusion Criteria

Study Design

Arm Groups

Study Contact