Celgene’s Pomalyst gets breakthrough therapy amrk from FDA for HIV-Positive and Negative Kaposi Sarcoma
Celgene plans additional studies with the AIDS Malignancy Consortiumin U.S. and sub-Saharan Africa
Pharmaceuticals, Biotechnology and Life Sciences
Celgene plans additional studies with the AIDS Malignancy Consortiumin U.S. and sub-Saharan Africa
Sesen bio to use the most recent analysis of its 12-monthPhase 3 VISTA trial data, which will be the basis for the meetings withthe FDA in May and June.
Acerus posts total revenues in Q1-2019 of $2.2 million, an increase of $0.5 millionor 33% compared to the first quarter of 2018 (“Q1-2018”).
The traditional R&D in the biopharmaceutical industry iswitnessing an upsurge, due to drug development research, which ishelping in the augmentation of the industrial microbiology market.
Eli Lilly’s Cyramza got its fifth FDA approval for in an advanced or metastatic cancer – this one for the second-line treatment of patients with hepatocellular carcinoma (HCC) who are AFP-High (AFP ≥400 ng/mL).
Food allergy has been essentially highly debatable for decades in atopicdermatitis, with some common food, including milk, egg, and soy. Thereis a lot of literature which provides evidence that common foodexacerbate atopic dermatitis.
Swedish Medivir said Monday that positive data from the investigator-initiated study of remetinostat in basal cell carcinoma (BCC) patients has shown that remetinostat gel offers a potentially effective and well-tolerated, non-surgical intervention for treatment of localized BCCs.
Transgene can start linical trial of its lead myvac™ candidate TG4050as a potential treatment for ovarian cancer patients after first-linesurgery and chemotherapy
TransPerfectLife Sciences, a leading provider of services and technologies tosupport global product development for the life sciences industry, hasreleased version 1.2 of myTI,the mobile application that enables real-time eTMF management andoversight for study teams on the go.
phase-II AMBER study whichdemonstrated that a significantly higher proportion of patients withresistant hypertension (RHTN) and chronic kidney disease (CKD) takingVeltassa® (patiromer) remained on spironolactone therapycompared to patients taking placebo at week 12.