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	Novavax applies for FDA emergency use authorization of its coronavirus vaccine Latest Corporate News; Pharma Jan1st/2022... Feb 01
	FDA approval for Moderna's Covid-19 vaccine Latest Corporate News ; Pharma... Feb 01
	FDA clears MindMed IND for MM-120 in treatment of generalized anxiety disorder FDA clearance leads to first commercial INDfor LSD, enabling initiation of Phase 2b dose-optimization trials of MM-120 in early 2022 - ... Jan 31
	SOM Biotech granted orphan drug designation by the FDA for SOM3355 Latest FDA approval news... Oct 20
	ImmixBio announces FDA Orphan drug designation for IMX-110 for the treatment of Soft Tissue Sarcoma Latest pharma news update... Oct 04
	U.S. FDA approves LIVMARLI (maralixibat) as the First and Only Approved Medication for the Treatment of Cholestatic Pruritus Indicated for patients with Alagille Syndrome one year of age and older... Oct 04
	FDA approves Abbott's Amplatzer Talisman System for PFO Closure in people at risk of recurrent Stroke Latest Pharma News update... Oct 04
	Versantis Receives U.S. FDA Orphan Drug Designation for VS-01 Latest pharma news updates... Sep 13
	Versantis receives U.S. FDA orphan drug designation for VS-01 Latest pharma news updates... Sep 09
	Poseida Therapeutics announces FDA clearance of investigational new drug application for P-BCMA-ALLO1, The new drug is an Allogeneic CAR-T Candidate for Relapsed/Refractory Multiple Myeloma... Sep 03
	PharmaTher Granted FDA Orphan Drug Designation For Ketamine To Treat Amyotrophic Lateral Sclerosis Latest Pharma News Update... Aug 07
	Alkermes Receives FDA fast track designation for Nemvaleukin Alfa for the treatment of Mucosal Melanoma FDA News Update... Aug 05
	FDA Clearance of IND for FPI-1966, Radiopharmaceutical for Head and Neck and Bladder Cancers Expressing FGFR3 Fusion Pharmaceuticals Announces FDA Clearance of IND for FPI-1966 ... Jul 30
	FDA Clearance of IND for FPI-1966, Radiopharmaceutical for Head and Neck and Bladder Cancers Expressing FGFR3 Fusion Pharmaceuticals Announces FDA Clearance of IND for FPI-1966 ... Jul 30
	Pfizer provides update on U.S. FDA review of Abrocitinib and XELJANZ filings Pharma News update... Jul 23
	Sanofi extends collaboration with Genedata for Pharmaceutical Development & Manufacturing Science Latest FDA approvals update... Jul 16
	Roche SARS-CoV-2 molecular test granted first FDA Emergency Use Authorization for PCR testing for Coronavirus Roche SARS-CoV-2 molecular test for PCR testing is effective for both symptomatic and asymptomatic Covid individuals ... Jun 22
	Bioheng Biotech received Orphan Drug Designation from the U.S. FDA for the treatment of T-ALL. New approval for treating leukomia... Jun 22
	Novartis receives FDA approval 177Lu-PSMA-617 for metastatic castration resistant prostate cancer FDA breakthrough therapy for Novartis metastatic prostate cancer drug ... Jun 21
	Boehringer Ingelheim's Investigational Treatment for Schizophrenia receives FDA Breakthrough Therapy Designation The company also announced the planned initiation of the innovative CONNEX Phase III clinical trial program assessing the safety and efficacy of BI 425809 ... May 27
	FDA authorizes monoclonal antibody therapy for emergency use in some patients 12 and older The authorization is specifically for those with mild-to-moderate Covid-19, who are at risk of getting much sicker... May 27
	FDA Emergency Use Authorization Approval for ZEUS ELISA SARS-CoV-2 Total Antibody Test System Now ELISA bases Covid test from Zeus Scientific... May 19
	US bans menthol and other flavored cigarettes CDC bans all flavored cigarettes... Apr 30
	Sorrento receives FDA clearance Phase 2 study for Sti-3031 ; Advanced Urothelial Carcinoma Sorrento intends to combine a variety of its proprietary mAbs in conjunction with the ADNAB technology platform... Apr 28
	FDA Approves GlaxoSmithKline's immunotherapy for Endometrial Cancer with specific biomarker GSK gets FDA nod for Jemperli indicated for endometrial cancer... Apr 26
25 Matching result(s) found!

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	AVEKSHA, four-day care centres, for the kids of industrial workers inauguratedApril 16, 2024
	Nearly a third of the constituencies have zero women candidates in Phase 1 and 2 of LS Elections; reveals The Quantum Hub’s Factsheet April 16, 2024
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Search Results

Novavax applies for FDA emergency use authorization of its coronavirus vaccine

FDA approval for Moderna's Covid-19 vaccine

FDA clears MindMed IND for MM-120 in treatment of generalized anxiety disorder

SOM Biotech granted orphan drug designation by the FDA for SOM3355

ImmixBio announces FDA Orphan drug designation for IMX-110 for the treatment of Soft Tissue Sarcoma

U.S. FDA approves LIVMARLI (maralixibat) as the First and Only Approved Medication for the Treatment of Cholestatic Pruritus

FDA approves Abbott's Amplatzer Talisman System for PFO Closure in people at risk of recurrent Stroke

Versantis Receives U.S. FDA Orphan Drug Designation for VS-01

Versantis receives U.S. FDA orphan drug designation for VS-01

Poseida Therapeutics announces FDA clearance of investigational new drug application for P-BCMA-ALLO1,

PharmaTher Granted FDA Orphan Drug Designation For Ketamine To Treat Amyotrophic Lateral Sclerosis

Alkermes Receives FDA fast track designation for Nemvaleukin Alfa for the treatment of Mucosal Melanoma

FDA Clearance of IND for FPI-1966, Radiopharmaceutical for Head and Neck and Bladder Cancers Expressing FGFR3

FDA Clearance of IND for FPI-1966, Radiopharmaceutical for Head and Neck and Bladder Cancers Expressing FGFR3

Pfizer provides update on U.S. FDA review of Abrocitinib and XELJANZ filings

Sanofi extends collaboration with Genedata for Pharmaceutical Development & Manufacturing Science

Roche SARS-CoV-2 molecular test granted first FDA Emergency Use Authorization for PCR testing for Coronavirus

Bioheng Biotech received Orphan Drug Designation from the U.S. FDA for the treatment of T-ALL.

Novartis receives FDA approval 177Lu-PSMA-617 for metastatic castration resistant prostate cancer

Boehringer Ingelheim's Investigational Treatment for Schizophrenia receives FDA Breakthrough Therapy Designation

FDA authorizes monoclonal antibody therapy for emergency use in some patients 12 and older

FDA Emergency Use Authorization Approval for ZEUS ELISA SARS-CoV-2 Total Antibody Test System

US bans menthol and other flavored cigarettes

Sorrento receives FDA clearance Phase 2 study for Sti-3031 ; Advanced Urothelial Carcinoma

FDA Approves GlaxoSmithKline's immunotherapy for Endometrial Cancer with specific biomarker

Trending Now