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Name/Company |
Approval Dates and Comments |
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Peginterferon alfa-2b
Sylatron™
Merck & Co Inc.
Schering Corporation
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The US FDA approved peginterferon alfa-2b in March 2011 to treat node-positive melanoma after surgical resection. Therapy is administered subcutaneously (may be self-injected) and is indicated as an adjuvant treatment of melanoma with microscopic or gross nodal involvement within 84 days of definitive surgical resection. The recommended dosing is 6 mcg/kg/week subcutaneously for 8 doses, followed by 3 mcg/kg/week subcutaneously for up to 5 years. A clinical investigation showed that patients who received the drug delayed cancer recurrence by approximately 9 additional months. One-third of peginterferon alfa-2b-treated patients ceased therapy due to adverse effects.
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Imiquimod 3.75% cream
Zyclara®
Graceway Pharmaceuticals
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The US FDA approved this immune response modifier in March 2011 for the topical treatment of external genital warts and perianal warts in patients ≥12 years of age. Under clinical investigation, Zyclara® showed that the once-daily treatment regimen for up to 8 weeks was safe and provided sustained efficacy. Only 15% of imiquimodtreated patients with complete clearance experienced recurrence 12 weeks after therapy.
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Adapalene 0.1% + benzoyl peroxide 2.5% gel
Tactuo™
Galderma Canada Inc.
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Health Protection Branch (HPB) of Health Canada approved a novel once-daily retinoid + benzoyl peroxide combination gel in March 2011 for the treatment of mild to moderate acne vulgaris in patients ≥12 years of age. The product is marketed in the US under the trade name of Epiduo®, which was FDA approved in December 2008.
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Collagenase clostridium histolyticum
Xiapex®
Pfizer Inc. BioSpecifics Technologies
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The European Medicines Agency (EMA) approved this novel, first-in-class biologic in March 2011 for the treatment of Dupuytren's contracture in adults with a palpable cord. The injected enzymes dissolve and weaken the contracted collagen cord. It is the only nonsurgical option for Dupuytren's disease.
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Generic Drug Update |
Minoxidil 5% foam
Perrigo Company
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The US FDA approved a generic version of OTC minoxidil foam in May 2011 for hair regrowth (innovator brand Men's Rogaine® Foam, McNeil-PPC, Inc.).
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Imiquimod 5% cream
Taro Pharmaceutical
Industries Ltd.
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The US FDA approved a generic version of imiquimod 5% cream in April 2011 for the topical treatment of actinic keratoses on the face or scalp, superficial basal cell carcinoma, and external genital and perianal warts in patients ≥12 years of age (innovator brand Aldara® 5% cream, Graceway Pharmaceuticals).
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Famciclovir tablets
Mylan Pharmacetuicals, Inc.
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A generic formulation of famciclovir (innovator brand Famvir®, Novartis Pharmaceuticals) was launched in April 2011 for the treatment of herpes zoster (shingles).
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Valacyclovir hydrochloride tablets
Actavis Group
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The US FDA has granted approval to Actavis Group in March 2011 to market its generic version of GlaxoSmithKline's antiviral product valacyclovir hydrochloride (Valtrex®) tablets for the treatment of herpes zoster and genital herpes.
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