Sun Pharma - Deuruxolitinib Approval To Strengthen Specialty Business: HDFC Securities

The brokerage expects specialty scale-up, traction in U.S. generics and new launches in India to drive growth and lead to a steady margin.

(Photo source: Sun Pharmaceutical Industries website)

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HDFC Securities Institutional Equities

Sun Pharmaceutical Industries Ltd. received timely approval from the U.S. Food and Drug Administration for its specialty drug Leqselvi (Deuruxolitinib – Janus kinase inhibitor) 8 mg tablets for the treatment of adults with severe alopecia areata (PDUFA in July 2024).

This will add to Sun Pharma a fast-growing derma-focused specialty business (existing brands like Ilumya and Winlevi). Deuruxolitinib (tablet) is poised to be a competitive product, offering better efficacy at the 24-week mark with 80% more scalp hair coverage for 30% of patients, compared to existing approved brands.

In contrast, Olumiant (Eli Lilly – baricitinib tablet) achieves this for 28% of patients, and Litfulo (Pfizer – ritlecitinib – capsule) for 23% of patients. We expect Deuruxolitinib to see a gradual scale-up over the next one-two years.

Sun Pharma has already developed its specialty infrastructure in the dermatology space, and it has started incurring costs for all pre-launch activities for Deuruxolitinib.

Sun Pharma will have five years of new chemical entity exclusivity. We expect specialty scale-up (traction in Ilumya, Winlevi, Cequa, Deuruxolitinib), traction in U.S. generics (100+ pending ANDA) and India (MR addition, new launches) to drive growth and lead to a steady margin (as growth offsets the increasing research and development).

We will factor in Deuruxolitinib post clarity on launch time and treatment regime price. We reiterate Buy with a target price of Rs 1,750, based on a 31 times Q1 FY27E earnings per share.

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HDFC Securities Institutional Equities Sun Pharma - Company Update.pdf
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