Drugs in the Pipeline
Soligenix announced that the FDA has granted Orphan Drug Designation to OrbeShield (oral beclomethasone 17,21-dipropionate or oral BDP) for the prevention of death following a potentially lethal dose of total body irradiation (TBI) during or after a radiation disaster.
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The FDA has approved the New Drug Application (NDA) for Emend (aprepitant; Merck) for oral suspension for the prevention of chemotherapy-induced nausea and vomiting (CINV) in patients aged ≥6 months old.
AAO-HNS 2021
Study authors conducted a prospective randomized trial to determine if there is a role for oral steroids in patients who have CRSsNP.
Drugs in the Pipeline
Soligenix announced today that the FDA has designated its OrbShield (oral beclomethasone 17, 21-dipropionate or oral BDP) development program for the treatment of Gastrointestinal Acute Radiation Syndrome (GI ARS), for Fast Track review.
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The team found no significant differences between the three groups of children who received topical steroid, emollient, or placebo in terms of Patient Oriented Eczema Measure scores.
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Taro Pharmaceuticals has received FDA approval for Flo-Pred (prednisolone acetate oral suspension), a prescription corticosteroid for the treatment of asthma, certain allergic and dermatologic conditions, and a variety of other indications.
Uncategorized
Both the 60- and 120-actuation sizes have been discontinued.
Slideshow
A white 24-year-old female presents with erythematous, papulopustular patches of skin in a muzzle-like distribution surrounding the mouth, chin, and glabellar region. Her history includes a variety of topical antibiotics that were previously successful with complete resolution; however, at present the lesions are persisting despite the treatment.
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Under drug interactions, new clinical comments regarding concomitant systemic/inhaled/nasal/ophthalmic corticosteroids have been added.
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Findings based on number of symptom-free days for daily versus as-needed treatment