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Trial record 1 of 2 for:    suvn-502
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Expanded Access to Provide SUVN-502 for the Treatment of Subjects With Alzheimer's Disease (SUVN-502)

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ClinicalTrials.gov Identifier: NCT03564964
Expanded Access Status : Available
First Posted : June 21, 2018
Last Update Posted : September 24, 2019
Sponsor:
Information provided by (Responsible Party):
Suven Life Sciences Limited

Tracking Information
First Submitted Date May 28, 2018
First Posted Date June 21, 2018
Last Update Posted Date September 24, 2019
 
Descriptive Information
Brief Title Expanded Access to Provide SUVN-502 for the Treatment of Subjects With Alzheimer's Disease
Brief Summary

This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to SUVN-502 for the treatment of Alzheimer's Disease. Investigator as well as the subject/caregiver must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the patient's medical history and program eligibility criteria.

Subjects will not be evaluated for efficacy and safety during the expanded access.

Detailed Description Not Provided
Study Type Expanded Access
Expanded Access Type Intermediate-size Population
Intervention Drug: SUVN-502
Tablet
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Expanded Access Status Available
Contacts
Contact: Ramakrishna Nirogi +91 9392483002 suvn502study@suven.com
Listed Location Countries Not Provided
Removed Location Countries  
 
Administrative Information
NCT Number NCT03564964
Responsible Party Suven Life Sciences Limited
Study Sponsor Suven Life Sciences Limited
Collaborators Not Provided
Investigators Not Provided
PRS Account Suven Life Sciences Limited
Verification Date September 2019