FDA grants priority review for Levo Therapeutics’ new drug application for LV-101 (intranasal carbetocin) for the treatment of Prader-Willi syndrome

6 July 2021 - Levo Therapeutics announced today that the U.S. FDA has granted priority review for its new drug application ...

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ANI Pharmaceuticals announces refiling of Cortrophin sNDA with FDA

6 July 2021 - ANI Pharmaceuticals today announced that the Company has re-filed its supplemental new drug application for Cortrophin Gel ...

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Provention Bio receives complete response letter to biologics license application for teplizumab for the delay of clinical type 1 diabetes in at-risk individuals

6 July 2021 - Previously reported pharmacokinetic drug product comparability considerations remain outstanding. ...

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FDA approves expanded indication for Merck’s Keytruda (pembrolizumab) in locally advanced cutaneous squamous cell carcinoma

6 July 2021 - Keytruda is now approved for the treatment of patients with recurrent or metastatic or locally advanced ...

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Athenex provides update from FDA Type A meeting regarding oral paclitaxel plus encequidar for the treatment of metastatic breast cancer

6 July 2021 - Athenex today announced that the Company held a Type A meeting with the U.S. FDA during the ...

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Opthea’s OPT-302 granted FDA fast track designation for wet age-related macular degeneration

6 July 2021 - FDA’s Fast Track Designation for OPT-302 offers benefits to expedite the OPT-302 Phase 3 clinical program and ...

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The controversial approval of an Alzheimer’s drug reignites the battle over the underlying cause of the disease

6 July 2021 - A new treatment targets amyloid clumps in the brain, but researchers have long debated whether that will ...

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It’s time for the FDA to fully approve the mRNA vaccines

1 July 2021 - Here’s a paradox: a new drug for Alzheimer’s disease, aducanumab, gets approved by the FDA through an ...

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Merck provides update on Keytruda (pembrolizumab) indication in third-line gastric cancer in the US

1 July 2021 - Merck today announced that the company plans to voluntarily withdraw the U.S. accelerated approval indication for Keytruda ...

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Statement for health care professionals: how COVID-19 vaccines are regulated for safety and effectiveness

5 July 2021 - Joint Statement from the International Coalition of Medicines Regulatory Authorities and World Health Organization. ...

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Medical devices reforms: enhancements to post-market monitoring

5 July 2021 - This project has been established to enhance the adverse event reporting processes. ...

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Sonic Healthcare USA to offer assay to aid in the selection of Jemperli (dostarlimab-gxly) therapy in endometrial cancer

2 July 2021 - LMC Pathology Services, a Sonic Healthcare USA Anatomic Pathology Practice, is the first reference laboratory in ...

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Galderma receives FDA approval for Restylane Contour for cheek augmentation and correction of midface contour deficiencies

29 June 2021 - Galderma's first and only product in the U.S. to use proprietary XpresHAn Technology for the cheeks. ...

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Iterum Therapeutics provides regulatory update

1 July 2021 - Iterum Therapeutics today announced that the Company received a letter from the U.S.FDA stating that, as ...

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Formycon and Bioeq announce submission of the marketing authorisation application for FYB201, a biosimilar candidate to Lucentis (ranibizumab) to the EMA

29 June 2021 - Formycon and its license partner Bioeq AG announce that the marketing authorisation application for FYB201, Formycon’s ...

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