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Anew Era TMS facilitates Treatment for medication-resistant depression
Anew Era TMS is a provider of transcranial magnetic stimulation TMS for treating individuals with medication-resistant depression and skin disorders. TMS offers and extends a safe and…
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Aeras declared results from Phase 2 TB Vaccine Trial for New BCG Revaccination Strategies
Non-profit organization, Aeras committed to developing vaccines against TB declared results from breakthrough Clinical Trial aiding evidence that TB Vaccines could forbid sustained…
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Roche set to acquire all shares of Flatiron Health from current 12.6%
Roche and Flatiron Health asserted that the two partners have ventured into a definitive agreement enumerating that Roche will acquire all shares of Flatiron Health from an existing…
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AbbVie asserts new results from the double-blinded of Phase 2 CELEST study
AbbVie asserted results from the double-blinded extension phase of the Phase 2 CELEST Study, exhibiting that many patients treated with upadacitinib who attained clinical response after…
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Novartis reports zero impact of Cosentyx on moderate to severe plaque psoriasis
Novartis declared additional results from the SCULPTURE study marking that two thirds of moderate to severe plaque psoriasis patients treated with Cosentyx exhibited zero impact of skin…
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Teva declares commercial availability of QVAR RediHaler Inhalation Aerosol
Teva Pharmaceutical Industries asserted the commercial availability of QVAR RediHaler Inhalation Aerosol to patients in both 40 mcg and 80 mcg strengths by prescription in the U.S QVAR…
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Banyan Biomarkers attained FDA’s De Novo request for Banyan BTI
Banyan Biomarkers asserted that the U.S FDA has extended De Novo request for the commercialization of Banyan BTI Brain Trauma Indicator), an in vitro diagnostic blood test to aid in the…
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Celgene Corporation asserted OTEZLA’s Phase II Clinical Trial data
Celgene Corporation asserted that data from a randomized, placebo-controlled, multi-center, phase II clinical trial of apremilast in patients with active ulcerative colitis who had…
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Arterys sought FDA clearance for Oncology AI suite
Arterys Inc declared its fifth 510 (k) clearance for Arterys Oncology AI suite and is milestone indicative of the company's momentum in applying AI to further medical imaging accuracy…
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Tusker Medical enlists first patient for OTTER Study
Tusker Medical announced the enrollment of first- in-office patients in the OTTER Study implied for Tusker's TULA (Tubes Under Local Anesthesia) System. Via an approved Investigational…
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Intralytix sought FDA clearance to begin Phase I/IIa Clinical Trials for bacteriophages
Intralytix proclaimed having sought Food and Drug Administration's clearance to commence Phase I/IIa Clinical Trials at Mount Sinai hospital in New York. Dating back to July,2015,…
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Servier and ImmunoQure partner to advance human Interferon-α autoantibody
ImmunoQure will collaborate with Servier to advance ImmunoQure's therapeutic human Interferon-α autoantibody through preclinical development and into the clinic where Servier will be…
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Bristol-Myers Squibb and Nektar Therapeutics collaborate commercially for NKTR-214
Bristol-Myers Squibb Company and Nektar Therapeutics collaborate commercially for Nektar's lead immuno-oncology program, NKTR-214.
The companies will jointly develop and…
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Sandoz asserts FDA’s approval for initiation of Glatopa
Novartis division, Sandoz asserted that the US FDA ha sanctioned the roll out and launch of Glatopa (glatiramer acetate injection) 40 mg/mL.
Glatopa was developed under a…
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FDA clearance sought for Roche’s Factor II and Factor V test on cobas 4800 system
Roche asserted that it has received FDA clearance for the cobas Factor II and Factor V Test for use on the cobas 4800 system. The test enables laboratories to simultaneously evaluate …
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Mallinckrodt affirms enlisting of first patient for ExpressGraft C9T1 Phase 1 Study
Mallinckrodt plc confirmed the enrollment of first patient for the company's Phase 1 study evaluating the safety and tolerance of ExpressGraft C9T1 skin tissue in the treatment of…
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PharmaMar signs licensing agreement with Seattle Genetics
PharmaMar forays into an exclusive licensing agreement with Seattle Genetics ensuring access to certain PharmaMar proprietary molecules for the development and commercialization of…
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Amgen’s BLINCYTO sBLA to be assessed by FDA for treating MRD
Amgen asserted that the Oncologic Drugs Advisory Committee of the U.S Food and Drug Administration will assess the data supporting the BLINCYTO supplemental Biologics License…
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Charles River Laboratories obtain MPI Research
Charles River Laboratories International declared that it has ventured into a definitive agreement to obtain MPI Research for $800 million in cash.
James C. Foster, Chairman and…
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SpinalCyte’s CybroCell Dermal Fibroblasts signals positive Phase 1/2 Clinical Trial Results
Degenerative disc disease has long been considered an inseparable part of aging but new breakthrough research from SpinalCyte suggests a new cell-based therapy could provide a cure for…
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