Allergan and Gedeon Richter receive U.S. FDA approval for expanded use of Vraylar (cariprazine) in the treatment of bipolar depression

28 May 2019 - New indication makes Vraylar first and only dopamine and serotonin partial agonist to treat the full spectrum ...

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RegenxBio announces first FDA approval of a gene therapy based on its proprietary NAV technology platform

24 May 2019 - FDA approval of Novartis' Zolgensma for the treatment of paediatric patients with SMA marks the first regulatory ...

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FDA approves Jakafi (ruxolitinib) for the treatment of patients with acute graft-versus-host disease

24 May 2019 - Jakafi is the first and only FDA approved treatment for patientswith steroid-refractory acute graft-versus-host disease. ...

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FDA approves first PI3K inhibitor for breast cancer

24 May 2019 - Today, the U.S. FDA approved Piqray (alpelisib) tablets, to be used in combination with the FDA-approved ...

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AveXis announces innovative Zolgensma gene therapy access programs for US payers and families

24 May 2019 - Annualised cost of Zolgensma is USD 425,000 per year for 5 years; 50% less than multiple established ...

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FDA approves innovative gene therapy to treat paediatric patients with spinal muscular atrophy, a rare disease and leading genetic cause of infant mortality

24 May 2019 - The U.S. FDA today approved Zolgensma (onasemnogene abeparvovec-xioi), the first gene therapy approved to treat children less ...

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FDA permits marketing of first diagnostic test to aid in detecting prosthetic joint infections

23 May 2019 - Today, the U.S. FDA permitted marketing of the Synovasure Lateral Flow Test Kit as an aid for ...

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Novartis CEO plans gene therapy price 'far lower' than $4 million to $5 million range

23 May 2019 - Novartis AG’s top executive said on Wednesday it expects to price its gene therapy for spinal ...

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Iovance Biotherapeutics announces breakthrough therapy designation for LN-145 for treatment of advanced cervical cancer patients who have progressed on or after chemotherapy

22 May 2019 - Iovance Biotherapeutics today announced that the U.S. FDA has granted breakthrough therapy designation to Iovance TIL therapy ...

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Avadel Pharmaceuticals announces FDA acceptance of new drug application for AV001

22 May 2019 - AV001 granted priority review. ...

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Agile Therapeutics announces FDA acceptance of the NDA resubmission of Twirla

22 May 2019 - FDA assigns Prescription Drug User Fee Act goal date of 16 November 2019. ...

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FDA approves Sorilux for adolescent plaque psoriasis

22 May 2019 - Mayne Pharma is pleased to announce that the US FDA has approved Sorilux (calcipotriene) foam, 0.005% ...

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House Committee proposes 6% increase in FDA funding for FY 2020

22 May 2019 - The House Appropriations Committee on Wednesday released a draft fiscal year 2020 funding bill for the ...

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U.S. FDA grants priority review of Invokana (canagliflozin) sNDA for the treatment of chronic kidney disease in patients with type 2 diabetes

22 May 2019 - Application was submitted in March 2019 based on landmark phase 3 CREDENCE renal outcomes study published in ...

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Lilly selling half-price version of popular Humalog insulin

22 May 2019 - A half-price version of Eli Lilly's popular Humalog insulin is now available, following the company's promise in ...

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