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FDA accepts new drug application from GBT's SCD therapy voxelotor
Time of Update: 2020-06-08
Global ( http:// announced that the u.S FDA (http:// had accepted the company's application for new drug (http:// (NDA) for the oral sickle cell anemia (SCD) treatment About Voxelotor Voxe
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Johnson and Johnson's Posson Tatterser gets NMPA approval to treat pulmonary hypertension in children
Time of Update: 2020-06-08
recently, Johnson and Johnson's Janssen Pharmaceutical (http:// company (http:// Actelion announced that Posson tatters (full-®, English brand name: Tracleer, generic name: bosentan) (spec: 32m
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Xuno Pharmaceuticals officially launched Abesta for treatment of lymphoma, renal cell carcinoma II, Phase III clinical
Time of Update: 2020-06-08
Recently, Abexinostat of Xuno Pharmaceuticals officially launched Phase II and III clinical treatment for lymphoma and renal cell carcinoma About Abestas Abes is the first candidate drug (http:
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Paclitaxel and encequidar combined to treat breast cancer in key phase 3 clinical study reached the main endpoint
Time of Update: 2020-06-08
Today, Athenex (http:// announce its oral formula, which combines paclitaxel and encequidar, to reach the main point in a key Phase 3 clinical study to treat metastatic breast cancer About Enceq
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AstraZeneca Tagrisso treats NSCLC patients with Phase 3 clinical trials with positive results
Time of Update: 2020-06-08
recently, AstraZeneca (http:// announced that its heavyweight third-generation EGFR inhibitor Tagrisso (osimertinib, oxitinib) has achieved positive results in the of a critical phase 3 clinical
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Karyopharm's innovative therapy Xpovio (selinexor) Phase 2b clinical trial yields positive results
Time of Update: 2020-06-08
recently, Karyopharm Therapeutics company (http:// announced positive results from the of its innovative clinical (http:// for the treatment of recurrent/incurable multiple myeloma study was
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FDA approves Novartis Beovu ® injection to treat wet macular degeneration
Time of Update: 2020-06-08
Novartis (http:// announced that the U.S Food drug (http:// Regulatory Authority ( FDA (http:// ) approved the Beovu ® , also known as RTH258, for the treatment of age-related wet macular deg
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FDA approves first triple-a-turalio (pexidartinib) for treatment of adult patients with symptomatic tendoncytoma
Time of Update: 2020-06-08
TGCT, also known as pigmentation fluffy conjure skateitis (PVNS), or tendon cytoblastoma (GCT-TS), is a rare non-malignant tumor with localized aggression Recently, the U.S FDA (http:// announce
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Intercept submits new drug Oberonic acid to FDA for new drug for FIbrosis caused by NASH
Time of Update: 2020-06-08
recently, Intercept submitted to the U.S FDA (http:// for the market of its new drug, http:// which is used in NASH-induced fibrosis Recently, the European Commission (EC) has approved the E
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FDA approves Xeris ready-to-use glutagon Gvoke injection application
Time of Update: 2020-06-08
recently, Xeris Pharmaceuticals announced that FDA (http:// approved its application for a market application for a ready-to-use glucagon Gvoke injection to treat severe hypoglycemia Gvoke has t
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FDA grants SpringWorks nirogacestat breakthrough treatment
Time of Update: 2020-06-08
hard fibroids are a rare soft tissue tumor that is deactivation and can lead to disfigurement It can quickly invade the surrounding healthy (http:// tissue, causing severe pain, internal bleeding
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CHMP recommends approval of Lonsurf for treatment of adult patients with metastatic stomach cancer
Time of Update: 2020-06-08
Recently, French drugmaker Servier and partner Tai ho Pharmaceutical http:// announced that the European Medicines (http:// Authority ( http:// Products (http:// Committee for human medicin
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Berry Bio Entekave generic spree application approved by FDA
Time of Update: 2020-06-08
Recently, the ubiah bio pharmaceutical (http:// (Suzhou) limited shares company (http:// of the Entikave tablets Pharmaceutical (http:// application (http:// was approved by the U.S Food M
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FDA approves Nabriva's innovative antibiotic Xenleta (lefamulin) for use in treatment of CABP
Time of Update: 2020-06-08
Community Acquired Bacterial Pneumonia (CABP), a bacterial pneumonia that is developed outside the hospital environment, is one of the most common infectious diseases that threatens health (http:/
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FDA grants LENVIMA and KEYTRUDA combination therapies for the treatment of hepatocellular cancer patients
Time of Update: 2020-06-08
recently, Aisho and Mershadon announced that the U.S Food medicine (http:// Regulatory Authority ( FDA (http:// ) has awarded LENVIMA (Chinese product name "LeWeima") and KEYTRUDA (Chinese commo
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FDA approves gene Tektrone (Merycin) in combination with glucocorticoids for use in children's GPA and MPA
Time of Update: 2020-06-08
recently, Swiss Pharmaceutical (http:// giant Roche's GeneTek announced that the U.S Food and Drug (http:// Authority ( FDA (http:// ) has approved Rituxan (Mera, rituximab, ritusxima) in co
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FDA grants Astex pharmaceutical anti-cancer drug ASTX727 orphan drug
Time of Update: 2020-06-08
recently, Japanese pharmaceutical company Otsuka Pharmaceuticals (http:// wholly-owned sub- company (http:// Astex Pharmaceuticals announced that the U.S Food and Drug (http:// Administrati
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FDA agrees to PharmaMar to file claim for new drug by Zepsyre ®
Time of Update: 2020-06-08
The u.S Food and drug (http:// Regulatory Authority ( FDA ) has agreed to approve The (http:// application for® a second-line single-drug treatment for small cell lung cancer, the of the F
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FDA grants Brynering Ingeheim's breakthrough therapy designation
Time of Update: 2020-06-08
today, the http:// of the of the of the bouring fdae company announced that the U.S FDA (http:// granted its small molecule tyrosine kinase inhibitor, Ofev (nintedanib), as a breakthrough ther
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FDA has granted Aeglea's Pegzilarginase Breakthrough Treatment
Time of Update: 2020-06-08
ARG1-D, also known as arginineemia, is a rare genetic disorder Patients due to mutations in the ARG1 gene, resulting in the lack of argininase 1 in the liver, arginine metabolism disorders Aeglea B