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Safety and Efficacy of VAY736 in Patients With Primary Sjogren's Syndrome (pSS)

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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

This study will determine the dose-response relationship of VAY736 for key efficacy and safety parameters

Eligibility

Eligible Ages: Between 18 Years and 75 Years
Eligible Genders: All
Accepts Healthy Volunteers: No

Inclusion Criteria

Exclusion Criteria

Study Design

Arm Groups

Study Contact

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Mary Woolsey
210-567-8049
woolseym@uthscsa.edu

Principal Investigator
Peter Fox

UT Health San Antonio

8403 Floyd Curl Dr
San Antonio, TX 78229

210-567-8555
IRBreliance@uthscsa.edu

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Safety and Efficacy of VAY736 in Patients With Primary Sjogren's Syndrome (pSS)

Lay Description

Category

Eligibility

Inclusion Criteria

Exclusion Criteria

Study Design

Arm Groups

Study Contact