News

May 11 2009

SkinMedica to Co-promote ACZONE® (dapsone) Gel 5% to Pediatricians in the U.S.

May 11 2009
CARLSBAD, CALIF. – May 11, 2009 – SkinMedica, Inc. today announced that it has entered into a co-promotion agreement with Allergan for ACZONE® (dapsone) Gel 5%, a first-in-class topical treatment for acne vulgaris. Representing the first new molecule in a decade approved by the FDA for the topical treatment of acne in patients 12 years of age and older, ACZONE® Gel 5% combines dapsone in a Solvent Microparticulate™gel, enabling dapsone to be applied topically in a well-tolerated formulation to provide patients with a convenient and effective therapy. Under the agreement, SkinMedica will exclusively promote ACZONE® Gel 5% to pediatricians in the United States through its existing sales force.
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Feb 23 2009

MAP Pharmaceuticals Announces Phase 3 Study of Unit Dose Budesonide in Children With Asthma Did Not Meet Primary Endpoints

Feb 23 2009
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Dec 19 2008

AstraZeneca and MAP Pharmaceuticals Announce Worldwide Collaboration to Develop and Commercialize Unit Dose Budesonide

Dec 19 2008
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Dec 11 2008

TRIA Beauty wins as the Prestige Skin Care Breakthrough Product of the Year

Dec 11 2008
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Dec 11 2008

Qnexa Meets Primary Endpoint by Demonstrating Superior Weight Loss over Components and Placebo in the 28-Week Equate Study (OB-301)

Dec 11 2008
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Dec 9 2008

Ambit Biosciences Presents Data on its Targeted Cancer Therapeutic AC220 for Acute Myeloid Leukemia

Dec 9 2008
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Dec 6 2008

Two Pralatrexate Studies Presented at the 50th Annual Meeting of the American Society of Hematology

Dec 6 2008
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Oct 26 2008

Paratek Reports Positive Phase 2 Clinical Data on its New Antibiotic PTK 0796 in Late Breaker Presentation at the 48th Annual Interscience Conference on Antimicrobial Agents and Chemotherapy

Oct 26 2008
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Oct 14 2008

Sirion Therapeutics Announces Positive Pivotal Uveitis Data For Durezol™

Oct 14 2008
Sirion Therapeutics, Inc., a privately held ophthalmic-focused biopharmaceutical company, announced preliminary results from a pivotal anterior uveitis trial that compared Durezol(TM) (difluprednate ophthalmic emulsion) 0.05% dosed four times daily (QID) to Pred Forte(R) (prednisolone acetate ophthalmic suspension) 1%, dosed eight times daily. Durezol is a topical ophthalmic corticosteroid indicated for the treatment of inflammation and pain associated with ocular surgery; it was approved by the US Food and Drug Administration in June 2008. Pred Forte(R) is the registered trademark of Allergan, Inc.
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Sep 17 2008

Auxilium Pharmaceuticals, Inc. Announces Initiation of XIAFLEX(TM) Phase IIb Study for Peyronie's Disease

Sep 17 2008
MALVERN, PA, Sep 17, 2008 (MARKET WIRE via COMTEX News Network) -- Auxilium Pharmaceuticals, Inc. (NASDAQ: AUXL), a specialty biopharmaceutical company, today announced that the first patients have been dosed in the Company's U.S. phase IIb trial of XIAFLEX(TM) for the treatment of Peyronie's disease. Peyronie's disease is the development of a collagen plaque, or scar tissue, on the shaft of the penis that hardens and reduces flexibility, causing the penis to bend or arc during erection resulting in psychological distress and pain for the patient and often interfering with or preventing intercourse.
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