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Study on teriflunomide in the treatment of multiple sclerosis

A multicenter, single-arm, prospective, real-world study on the efficacy, safety and tolerability of teriflunomide tablets in Chinese patients with multiple sclerosis

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120683
Enrollment
Unknown
Registered
2026-03-18
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple sclerosis

Interventions

The teriflunomide treatment group:None

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years old, no gender restrictions; 2.Signing the informed consent form means that one can understand and comply with all the requirements of the research; 3.Diagnosed with relapsing multiple sclerosis according to the Chinese Guidelines for the Diagnosis and Treatment of Multiple Sclerosis (2023 Edition); 4.Receive treatment with teriflunomide; It is necessary to take Teriflunomide tablets (the prescription is issued by a doctor according to their clinical practice), and whether to prescribe Teriflunomide tablets is not related to the decision to include the patient in the current study.

Exclusion criteria

Exclusion criteria: 1.Currently participating in or having participated in any other interventional clinical trials within the past six months. 2.Women who are preparing for pregnancy, pregnant or breastfeeding; 3.Have a history of other active malignant diseases within 2 years before entering the study; 4.According to the investigator's judgment, the subject is not suitable for study observation; 5.Age over 75 years (including 75 years).

Design outcomes

Primary

MeasureTime frame
The incidence of adverse reactions;Annual recurrence rate;

Secondary

MeasureTime frame
Severity of the disease;The types and incidence rates of new adverse reactions;

Countries

China

Contacts

Public ContactYong Zhang

The Affiliated Hospital of Xuzhou Medical University

zy20037416@163.com+86 516 85802033

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026