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U.S. Food and Drug Administration approval of the Gardasil 9 human papillomavirus vaccine has been expanded to include people ages 27 through 45

FDA Approves HPV Vaccine for People Through Age 45

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Updated vaccine designed to prevent cancers and disease caused by nine HPV types
Libtayo (cemiplimab-rwlc) injection has been approved by the U.S. Food and Drug Administration to treat metastatic cutaneous squamous cell carcinoma

FDA Approves New Treatment for Squamous Cell Carcinoma

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Libtayo is the sixth FDA-approved immune checkpoint inhibitor targeting the PD-1 pathway
Arikayce (amikacin liposome inhalation suspension) has been approved by the U.S. Food and Drug Administration to treat lung disease caused by Mycobacterium avium complex bacteria among patients who do not respond to conventional therapies

FDA Approves New Drug for Antibiotic-Resistant Lung Disease

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Arikayce approved to treat lung disease caused by Mycobacterium avium complex bacteria
The PK Papyrus Covered Coronary Stent System has been approved by the U.S. Food and Drug Administration to treat acute coronary artery perforations.

FDA Approves Device for Acute Coronary Artery Perforations

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The PK Papyrus device is a balloon-expandable covered coronary stent and delivery system
Lumoxiti (moxetumomab pasudotox-tdfk) injection has been approved to treat certain instances of relapsed or refractory hairy cell leukemia

FDA Approves Novel Treatment for Hairy Cell Leukemia

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Lumoxiti, a CD22-directed cytotoxin, approved for adults who have had at least two prior therapies
Cassipa (buprenorphine and naloxone)

FDA Approves New Treatment for Opioid Dependence

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The sublingual buprenorphine and naloxone combo should be part of a complete treatment plan
Oxervate (cenegermin) has been approved by the U.S. Food and Drug Administration to treat neurotrophic keratitis

FDA Approves First Drug for Neurotrophic Keratitis

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Oxervate, a topical eye drop, led to complete corneal healing among 70 percent of study participants
Poteligeo (mogamulizumab) injection has been approved by the U.S. Food and Drug Administration to treat adults with two rare types of non-Hodgkin lymphoma.

FDA Approves Poteligeo for Rare Types of Non-Hodgkin Lymphoma

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Drug approved to treat relapsed or refractory mycosis fungoides and Sézary syndrome
Azedra (iobenguane) has been approved by the U.S. Food and Drug Administration to treat people 12 and older with rare adrenal gland tumors (pheochromocytoma or paraganglioma) that can't be surgically removed and have spread beyond the original site.

FDA Approves Azedra for Rare Adrenal Tumors

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First systemic treatment for patients who experience tumor-related symptoms such as hypertension
A magnetic system for guiding lymph node biopsies in patients with breast cancer undergoing mastectomy has been approved by the U.S. Food and Drug Administration.

FDA Approves Magnetic System for Guiding Lymph Node Biopsies

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Sentimag System uses magnetic detection to identify sentinel lymph nodes for surgical removal