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Sirolimus topical - Palvella Therapeutics/TransDerm

Drug Profile

Sirolimus topical - Palvella Therapeutics/TransDerm

Alternative Names: PTX 022; QTORIN™ 3.9% rapamycin; QTORIN™ 3.9% rapamycin anhydrous gel; Rapamycin topical - Palvella Therapeutics/TransDerm; TD201

Latest Information Update: 05 Dec 2023

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At a glance

  • Originator Palvella Therapeutics; TransDerm
  • Class Anti-infectives; Anti-inflammatories; Antiepileptic drugs; Antifungals; Antineoplastics; Cardiovascular therapies; Eye disorder therapies; Lactones; Macrolides; Nootropics; Polyenes; Pyridines; Skin disorder therapies
  • Mechanism of Action Immunosuppressants; Methylmalonyl CoA mutase stimulants; MTOR protein inhibitors; T lymphocyte inhibitors
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Pachyonychia congenita
  • New Molecular Entity No
  • Available For Licensing Yes

Highest Development Phases

  • Phase III Pachyonychia congenita
  • Phase II Basal cell nevus syndrome; Lymphangioma

Most Recent Events

  • 01 Dec 2023 Palvella Therapeutics has patent pending for anhydrous gel formulations of rapamycin in Europe, and Japan
  • 01 Dec 2023 Palvella Therapeutics has patent protection for Sirolimus topical in Japan
  • 16 Nov 2023 Sirolimus topical - Palvella Therapeutics/TransDerm receives Breakthrough Therapy status for Lymphangioma in USA
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