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Johnson & Johnson Pulls Neutrogena and Aveeno Spray Sunscreens Over Benzene Contamination

XTalks

Related: Google Launches AI-Based Dermatology Assist Tool. In 2019, lots of losartan potassium/hydrochlorothiazide were recalled after they were found to contain above acceptable levels of the suspected cancer-causing compound N-Nitroso-N-methyl-4-aminobutyric acid (NMBA). Benzene is a colorless flammable liquid that has a sweet odor.

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Ycanth (Cantharidin) Revolutionizes Molluscum Contagiosum Treatment with FDA Approval

XTalks

Verrica, a company specializing in dermatology therapeutics, has designed Ycanth to be delivered through a single-use applicator. ’s berdazimer gel, containing 10.3 Ycanth (cantharidin) topical solution, developed by Verrica Pharmaceuticals Inc., Another noteworthy contender is Novan Inc.’s

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Crescita Announces Licensing Agreement for Pliaglis; in China

The Pharma Data

(TSX: CTX) (OTC US: CRRTF) (“Crescita” or the “Company”), a growth-oriented, innovation-driven Canadian commercial dermatology company with in-house research & development (“R&D”) and manufacturing capabilities, today announced that it has entered into an exclusive agreement with Juyou-Biotechnology Co.

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FDA Approves Klisyri (tirbanibulin) for the Treatment of Actinic Keratosis on the Face or Scalp

The Pharma Data

Klisyri will be manufactured by Athenex, highlighting the vertically integrated capabilities of the company ranging from a preclinical lead to a developed product for market launch. We invest in differentiated and groundbreaking medical dermatology products to bring our innovative solutions to patients in need.

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Johnson & Johnson to Acquire Momenta Pharmaceuticals, Inc., Expanding Janssen’s Leadership in Novel Treatments for Autoimmune Diseases

The Pharma Data

Nipocalimab gives Janssen the opportunity to reach significantly more patients by pursuing indications across many autoimmune diseases with substantial unmet medical need in maternal-fetal disorders, neuro-inflammatory disorders, rheumatology, dermatology and autoimmune hematology. Food and Drug Administration. An estimated 2.5

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FDA Grants Priority Review and EMA Accepts Regulatory Submission for Pfizer’s Abrocitinib, an Oral Once-Daily JAK1 Inhibitor, for Patients 12 and Up with Moderate to Severe Atopic Dermatitis

The Pharma Data

They need additional treatment options that alleviate the symptoms most important to them,” said Jonathan Silverberg, MD, PhD, MPH, Department of Dermatology, The George Washington University School of Medicine and Health Sciences. DISCLOSURE NOTICE: The information contained in this release is as of October 27, 2020. Dermatology.

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FDA approves Octapharma’s Octagam® 10% for adult dermatomyositis

Bioengineer

Renal dysfunction and acute renal failure occur more commonly in patients receiving IGIV products containing sucrose. Octagam® 10% does not contain sucrose. For patients at risk of thrombosis, renal dysfunction or renal failure, administer Octagam® 10% at the minimum infusion rate practicable. About the Octapharma Group.