Naratriptan

Naratriptan (trade names include Amerge and Naramig) is a triptan drug marketed by GlaxoSmithKline and is used for the treatment of migraine headaches. Naratriptan is available in 2.5mg tablets. It is a selective 5-HT1 receptor subtype agonist.

CAS# 121679-13-8

Naratriptan
Naratriptan

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Selumetinib

Selumetinib (AZD6244) is a drug that was discovered by Array BioPharma and was licensed to AstraZeneca. It is being investigated for the treatment of various types of cancer, such as non-small cell lung cancer (NSCLC).

CAS# 606143-52-6

606143-52-6
Selumetinib

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ILUMYA

Sun Pharma announced that the US FDA has approved the marketing of its new drug ILUMYATM (tildrakizumab-asmn) to treat adult patients with moderate to severe plaque psoriasis who are eligible for systemic therapy or phototherapy.

Sun Pharma

Psoriasis is a chronic immune disease that occurs on the skin. It is a non-communicable disease that accelerates the growth cycle of skin cells and causes the appearance of thick scaly areas on the skin. Plaque psoriasis usually manifests itself as a red, raised skin area covered with flaky white scales, which can cause itching, pain and can lead to dehiscence and bleeding. Many patients need to continue living in the pain caused by this disease. They urgently need effective treatments to relieve the disease and improve the quality of life.

We congratulate the approval of this new drug and expect it to bring relief to psoriasis patients.

GREAT

 

Prazosin hydrochloride

Prazosin Hypovase is a sympatholytic drug used to treat high blood pressure, anxiety, and posttraumatic stress disorder (PTSD). It is an α1-blocker which acts as an inverse agonist at alpha-1 adrenergic receptors. These receptors are found on vascular smooth muscle, where they are responsible for the vasoconstrictive action of norepinephrine. They are also found throughout the central nervous system.

CAS# 19237-84-4

Prazosin
Prazosin

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Novartis wins FDA nod for newly acquired cancer drug Lutathera

Just months after picking up Advanced Accelerator Applications in a $3.9 billion buyout, Novartis is getting a quick boost with the U.S. approval for Lutathera. The FDA approved the first-in-class med as a treatment for rare cancers of the digestive tract the other day.

Lutathera is first the peptide receptor radionuclide therapy to win U.S. approval, according to a release from AAA. Approved to treat somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (GEP-NETs), the drug works by binding to the receptors and then using radiation to fight cancer.

Jefferies analysts have predicted $500 million to $1 billion in peak sales for the drug, while Baader Helvea analyst Bruno

NovartisBulic has been more optimistic. At the time of the AAA acquisition by Novartis last year, he predicted $2 billion in peak sales, according to Reuters.