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Study identifier: NCT07583251 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Safety And Tolerability Of Gamma Glutamylcysteine (GGC) Oral Supplementation In MCI Patients

Condition: Mild Cognitive Impairment (MCI)  ·  Sponsor: Pravat Mandal

PhasePhase 1
Planned participants9
Who can joinAll sexes, 55 Years to 80 Years
Healthy volunteersNo

About this study

The goal of this study is to evaluate the safety and tolerability of Gamma Glutamylcysteine (GGC) supplement at different doses (400mg/day or 800mg/day or 1200mg/day) when administered orally to patients with MCI over 3 months. This study is designed to generate preliminary clinical safety data to inform the feasibility and design of larger controlled trials.

This description comes directly from the study's public registry record.

Talk to the study team

Pravat Pravat K MANDAL  ·  4126999561  ·  mandalpk@pitt.edu

Nazia Pillar  ·  878-670-3123  ·  clinic55@pitt.edu

Always discuss trial participation with your own doctor first.

Locations (1)

UPMC Presbyterian HospitalPittsburgh, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07583251