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The U.S. Food and Drug Administration has approved Zarxio (filgrastim-sndz)

FDA Approves First Biosimilar Drug in U.S.

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Zarxio is highly similar to long-sanctioned cancer drug
U.S. Food and Drug Administration approval of Opdivo (nivolumab) has been expanded to include advanced non-small-cell lung cancer

FDA: Opdivo Approval Expanded to Include Lung Cancer

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FDA approves drug for NSCLC patients who have been treated with platinum-based chemotherapy
The combination antibiotic Avycaz (ceftazidime-avibactam) has been approved by the U.S. Food and Drug Administration to treat adults with complicated infections of the intra-abdominal area or urinary tract

FDA Approves New Combination Antibiotic Avycaz

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Combination drug sanctioned for abdominal, urinary tract infections
Farydak (panobinostat) has been approved by the U.S. Food and Drug Administration to treat multiple myeloma. Farydak inhibits the activity of histone deacetylases

FDA Approves Farydak for Multiple Myeloma

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Drug is sanctioned for people who have received at least two prior standard therapies
The VenaSeal closure system has been approved by the U.S. Food and Drug Administration to treat superficial varicose veins of the legs that cause symptoms.

FDA: New Device Treats Superficial Varicose Veins

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Seals the affected superficial veins using an adhesive agent
The U.S. Food and Drug Administration has allowed marketing of the Eclipse System for the treatment of fecal incontinence in adult women aged 18 to 75

FDA Permits Marketing of Device for Female Fecal Incontinence

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Use of Eclipse System led to 50 percent decrease in episodes
The kinase inhibitor Lenvima (lenvatinib) has been approved by the U.S. Food and Drug Administration to treat differentiated thyroid cancer that has progressed despite radioactive iodine therapy

FDA Approves Lenvima for Type of Thyroid Cancer

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To treat differentiated thyroid cancer that has progressed despite radioactive iodine therapy
The ENROUTE Transcarotid Neuroprotection System has been approved by the U.S. Food and Drug Administration as a minimally invasive device designed to help prevent stroke during stent and angioplasty procedures.

FDA OKs Device to Help Prevent Procedure-Related Stroke

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Transcarotid system designed to help prevent stroke during stent and angioplasty procedures
The U.S. Food and Drug Administration has expanded the approved use for Lucentis (ranibizumab injection) 0.3 mg to treat diabetic retinopathy in patients with diabetic macular edema.

FDA Expands Approval of Lucentis for Diabetic Retinopathy

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To treat diabetic retinopathy in patients with diabetic macular edema
Ibrance (palbociclib) has been approved by the U.S. Food and Drug Administration to treat advanced breast cancer among postmenopausal women.

FDA Approves Ibrance to Treat Advanced Breast Cancer

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For postmenopausal women with ER+, HER2− metastatic breast cancer