Sun Pharma reports sustained LEQSELVI efficacy in two-year alopecia study
- Sun Pharma presented seven LEQSELVI studies at EADV Congress 2026
- 93.9% of baseline responders maintained scalp hair regrowth at Week 108
- 76.6% of baseline nonresponders achieved response by Week 52
- Safety profile remained consistent with no major cardiovascular events reported
- Data supports LEQSELVI as a long-term treatment option for severe alopecia areata

*this image is generated using AI for illustrative purposes only.
Sun Pharmaceutical Industries Limited announced that new long-term data for LEQSELVI (deuruxolitinib) demonstrated sustained efficacy and safety in adults with severe alopecia areata. The findings were presented at the European Academy of Dermatology and Venereology (EADV) Congress 2026, highlighting durable hair regrowth over a two-year period.
The featured oral presentation reported results from an open-label extension study evaluating treatment up to two years. The safety profile remained generally consistent with previous clinical experience. Most treatment-emergent adverse events were mild or moderate, and discontinuations due to adverse events were uncommon. No deaths, thrombosis, or major adverse cardiovascular events were reported among patients receiving the FDA-approved dose of 8 mg twice-daily.
Long-term efficacy outcomes
Analyses presented in a poster indicated durable scalp hair regrowth through Week 108 in patients receiving LEQSELVI in the European open-label extension. Among baseline responders who maintained their response at Week 52 and continued in the study, 93.9% maintained that response at Week 108. Additionally, 76.6% of baseline nonresponders achieved a response by Week 52. Of those who achieved this response and continued, 96.8% maintained it at Week 108.
| Patient Group | Metric | Outcome |
|---|---|---|
| Baseline Responders | Response maintained at Week 108 | 93.9% |
| Baseline Nonresponders | Achieved response by Week 52 | 76.6% |
| Nonresponders converting to responders | Response maintained at Week 108 | 96.8% |
Clinical significance and portfolio context
Arash Mostaghimi, Vice Chair of Clinical Trials and Innovation at Brigham and Women’s Hospital, noted that severe alopecia areata is a chronic autoimmune disease where long-term treatment considerations are critical. He stated that the data reinforce the growing body of evidence supporting LEQSELVI as a long-term treatment option. Ahmad Naim, Senior Vice President and North America Chief Medical Officer at Sun Pharma, emphasized that the data expand understanding beyond initial treatment response to include long-term tolerability and durability of benefit.
The company presented seven presentations on LEQSELVI at the congress, which was part of 22 total presentations from Sun Pharma across its dermatology and immunology portfolio. Pooled post hoc analyses of THRIVE-AA1 and THRIVE-AA2 trials showed consistent efficacy across clinically relevant subgroups, including patients with eyebrow, eyelash, or nail involvement.
What the numbers show
The data reveals a strong conversion rate from non-response to response within the first year, with 76.6% of initial nonresponders achieving clinical success by Week 52. This high conversion rate suggests that a significant portion of the patient population may derive benefit even if they do not respond immediately. Furthermore, the high maintenance rates (93.9% and 96.8%) among responders indicate that once clinical benefit is established, it is highly likely to persist over the two-year observation period, addressing a key concern in chronic autoimmune management.
Historical Stock Returns for Sun Pharmaceutical
| 1 Day | 5 Days | 1 Month | 6 Months | 1 Year | 5 Years |
|---|---|---|---|---|---|
| -0.86% | -3.43% | -6.20% | +2.49% | +12.96% | +120.10% |
How will Sun Pharma leverage the 93.9% long-term response maintenance rate to differentiate LEQSELVI from existing JAK inhibitors in payer negotiations and formulary placements?
What are the specific commercialization strategies for expanding LEQSELVI's indication to pediatric populations or other autoimmune conditions based on this two-year safety data?
Given the high conversion rate of nonresponders by Week 52, how might clinical guidelines evolve regarding the recommended duration of trial therapy before declaring treatment failure?


































