Tofacitinib in Patients With Amyotrophic Lateral Sclerosis

EARLY_PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

December 1, 2024

Primary Completion Date

December 1, 2025

Study Completion Date

June 1, 2026

Conditions
Amyotrophic Lateral Sclerosis
Interventions
DRUG

Tofacitinib tablets

All patients should be closely monitored for signs and symptoms of infection during and after treatment with tofacitinib tablets. If a patient develops a severe infection, opportunistic infection, or sepsis, medication should be discontinued. During treatment, patients with lymphocyte counts \< 500 cells/mm\^3 or ANC \< 500 cells/mm\^3 confirmed by repeated testing should be stopped. When 500≤ANC≤1000 cells/mm\^3, administration should be interrupted, and if ANC returns to more than 1000 cells/mm\^3, administration should be resumed. When hemoglobin \< 8 g/dL or decreases by more than 2 g/dL, administration should be interrupted until hemoglobin values return to normal.

Trial Locations (1)

100050

Beijing Tiantan Hospital, Beijing

All Listed Sponsors
collaborator

Turing-Darwin Laboratory; West Institute of Computing Technology, Chongqing, China

UNKNOWN

lead

Beijing Tiantan Hospital

OTHER