CompletedPhase 1NCT07154095

A Single-Center, Randomized, Open-Label, Two-Sequence, Two-Period, Crossover Study Comparing the Pharmacokinetics and Safety of Pyridostigmine Sustained-Release and Immediate-Release Tablets Following Single and Multiple Doses in Healthy Chinese Participants

Studying Adult-onset myasthenia gravis

Last synced from ClinicalTrials.gov

Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing data

Key facts

Sponsor
West China Second University Hospital
Principal Investigator
Yu Qin, M.D
China West China Second University Hospital Chengdu, China
Intervention
Sustained-Release Tablets(drug)
Enrollment
40 enrolled
Eligibility
18-45 years · All sexes
Timeline
20232024

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07154095 on ClinicalTrials.gov

Other trials for Adult-onset myasthenia gravis

Additional recruiting or active studies for the same condition.

See all trials for Adult-onset myasthenia gravis

← Back to all trials