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Rezurock in India

How patients in India access Rezurock (belumosudil) via Named Patient Program.

Rezurock - overview

Rezurock (belumosudil) is manufactured by Sanofi / Kadmon and indicated for Chronic graft-versus-host disease, >=12 yrs. It is an oral small molecule (ROCK2 inhibitor) approved by the US FDA in 2021 and may be accessible to patients in India through a Named Patient Program or personal-import pathway.

Access in India

India's CDSCO permits import of unapproved drugs under Rule 36 for personal use by patients with a prescription from a registered medical practitioner. Named Patient import is common for rare-disease indications.

How Reserve Meds coordinates access in India

  1. Patient or treating physician submits a request.
  2. We verify clinical appropriateness and India-specific eligibility.
  3. Treating physician in India issues prescription and clinical justification.
  4. Country-specific NPP/personal-import forms are prepared and filed.
  5. We source Rezurock from a DSCSA-compliant US specialty wholesaler.
  6. Cold-chain shipment to the patient's physician or hospital pharmacy in India.

Typical timeline for India

End-to-end, most requests are completed in 2-6 weeks. India's tier 1 regulatory maturity typically supports fast processing times.

What patients and physicians in India ask

  • Is the pathway legal in India? Yes - it operates under India's established NPP or personal-import framework.
  • Does my insurance cover it? Typically no for NPP drugs; patient prepayment is standard.
  • What physician credentials do I need? A licensed physician in India able to issue the prescription and clinical justification.
  • What if the drug is in shortage? We will inform you upfront and decline rather than promise what we cannot deliver.
  • Can I re-supply? Yes - for chronic therapies we arrange ongoing re-supply.

Start a request for Rezurock in India

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YELLOW
AI Regulatory Review Agent, preliminary signal
Biologic drug requires CDSCO import confirmation for the specific patient indication. Cold-chain shipping validated. Typically 2-4 week approval.
Rule: biologic_moh_confirmation • Reviewed 2026-04-22

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Review & oversight. Content on this page is reviewed by Reserve Meds's clinical and regulatory team. A US-licensed pharmacist reviews every prescription before dispensing. Regulatory posture is informational, not legal advice; case-specific questions route to retained outside counsel. Review methodology ›
Last medically reviewed: .