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Efficacy and Safety Profile of Oral Tofacitinib in Non-Segmental Vitiligo
Soumya Jagadeesan1, Neenu Prasad1, Prasanna Duraiswamy2
1From the Department of Dermatology, Amrita Institute of Medical Sciences and Research Centre, Amrita Vishwa Vidyapeetham, Ponekkara, Kochi, Kerala, India.
Background:
Vitiligo is a chronic disease that is often challenging to treat. Melanocyte destruction in vitiligo is mediated by immune pathways involving IFN-γ and CD8+ T cells. Tofacitinib, a Janus kinase (JAK) 1/3 inhibitor, can be a promising treatment for vitiligo due to its potential to inhibit IFN-γ signaling. We retrospectively reviewed the records of 16 patients (6 men, 10 women; mean age 39.7 years) with nonsegmental vitiligo refractory to conventional therapies who were treated with oral tofacitinib along with topical tacrolimus and phototherapy.
Aims:
To evaluate the efficacy and adverse effects of the JAK1/3 inhibitor, oral tofacitinib, in the treatment of nonsegmental vitiligo.
Methods:
We retrospectively reviewed the records of 16 patients (6 men, 10 women; mean age: 39.7 years) with nonsegmental vitiligo refractory to conventional therapies who were treated with oral tofacitinib along with topical tacrolimus and phototherapy. Improvement was assessed using Vitiligo Area Scoring Index (VASI) at weeks 6, 12, and 24. Hemogram, lipid profile, liver, and renal function tests were monitored during the treatment period.
Results:
Improvement was assessed using Vitiligo Area Scoring Index (VASI) at weeks 6, 12, and 24. Mean VASI scores improved from 5.038 at baseline to 1.269 at 24 weeks, with 13 patients (81.25%) achieving at least 50% improvement. Transient leukopenia was observed in 3 patients, and one patient developed palmar warts.
Conclusions:
Oral tofacitinib shows significant potential in the management of nonsegmental vitiligo, in patients unresponsive to conventional therapies especially in combination with phototherapy. No significant adverse effects were observed during the follow up period other than a transient leukopenia in three patients and palmar warts in one patient.
Insights
Tofacitinib, a JAK inhibitor, shows promise for treating nonsegmental vitiligo unresponsive to traditional therapies. This study found significant VASI score improvement with manageable side effects in patients treated with tofacitinib.
Area of Science:
- Dermatology
- Immunology
- Pharmacology
Background:
- Vitiligo is a chronic autoimmune condition causing melanocyte destruction.
- Immune pathways involving IFN-γ and CD8+ T cells mediate vitiligo pathogenesis.
- Tofacitinib, a Janus kinase (JAK) 1/3 inhibitor, may target IFN-γ signaling in vitiligo.
Purpose of the Study:
- To assess the efficacy and safety of oral tofacitinib for nonsegmental vitiligo.
- To evaluate tofacitinib's effectiveness in patients refractory to conventional treatments.
Main Methods:
- Retrospective review of 16 patients with nonsegmental vitiligo.
- Patients received oral tofacitinib combined with topical tacrolimus and phototherapy.
- Vitiligo Area Scoring Index (VASI) assessed improvement at 6, 12, and 24 weeks.
Main Results:
- Mean VASI scores decreased from 5.038 at baseline to 1.269 at 24 weeks.
- 81.25% of patients achieved at least 50% VASI improvement.
- Adverse effects included transient leukopenia (3 patients) and palmar warts (1 patient).
Conclusions:
- Oral tofacitinib demonstrates significant potential for managing nonsegmental vitiligo, particularly in combination therapy.
- Tofacitinib offers a viable treatment option for refractory vitiligo cases.
- The treatment exhibited a favorable safety profile with manageable adverse events.
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