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PharmaShots Weekly Snapshots (September 16 – September 20, 2024)

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PharmaShots Weekly Snapshots (September 16 – September 20, 2024)

This week PharmaShots’ news was all about the updates on Clinical Trials, Pharma, Biotech, COVID-19, Regulatory & MedTech. Check out our full report below:

 

Novartis to Highlight Updated Data from the P-III (NATALEE) Study of Kisqali (Ribociclib) for Treating Early Breast Cancer (EBC) at ESMO 2024

Read More: Novartis                                                                                 

Merck Highlights 10 Years Data from the P-III (KEYNOTE-006) Study of Keytruda in Advanced Melanoma Patients at ESMO 2024

Read More: Merck                                                                                             

Boehringer Ingelheim Reports the P-III (FIBRONEER-IPF) Trial Data of Nerandomilast to Treat Idiopathic Pulmonary Fibrosis (IPF)

Read More: Boehringer Ingelheim                                                                           

Merck and Daiichi Sankyo Report the P-III (HERTHENA-Lung02) Study Data of Patritumab Deruxtecan to Treat Non-Small Cell Lung Cancer

Read More: Merck & Daiichi Sankyo                                                            

Johnson & Johnson Reports the P-II (SunRISe-4) Study Data of TAR-200 Plus Cetrelimab to Treat Muscle-Invasive Bladder Cancer

Read More: Johnson & Johnson                                                                                  

Roche Reports Topline Data from P-III (CENTERSTONE) Study of Xofluza to Reduce the Transmission of Influenza Virus

Read More: Roche                                                                                            

GSK Reports Topline Results from the P-III Trial of Arexvy Co-Administered with Shingrix

Read More: GSK                                                                                                           

Satellos Reports the First Patient Dosing with SAT-3247 in P-I Trial for Duchenne Muscular Dystrophy

Read More: Satellos                                                                                                       

Sanofi Reports the P-III (HERCULES) Study Results of Tolebrutinib for Treating Non-Relapsing Secondary Progressive Multiple Sclerosis (nrSPMS)

Read More: Sanofi                                                                                                        

 

Eli Lilly’s Ebglyss (L ebrikizumab-lbkz) Receives the US FDA’s Approval for Treating Moderate-to-Severe Atopic Dermatitis

Read More: Eli Lilly                                                                                                       

Sanofi and Regeneron’s Dupixent Receives the US FDA’s Approval to Treat Adolescents with Chronic Rhinosinusitis with Nasal Polyps (CRSwNP)

Read More: Sanofi & Regeneron                                                                         

Roche Reports the US FDA’s Approval of Ocrevus Zunovo for Treating Relapse and Progressive Multiple Sclerosis

Read More: Roche                                                                                                    

GSK Reports the NDA Acceptance of Blenrep Combinations by the Japanese MHLW for R/R Multiple Myeloma

Read More: GSK                                                                                                         

Poseida Therapeutics’ P-BCMA-ALLO1 Gains the US FDA’s Regenerative Medicine Advanced Therapy Designation for R/R Multiple Myeloma

Read More: Poseida Therapeutics                                                                           

AstraZeneca’s Fasenra Receives the US FDA’s Approval for the Treatment of Eosinophilic Granulomatosis with Polyangiitis

Read More: AstraZeneca                                                                                             

Merck Reports the US FDA’s Approval of Keytruda Plus Pemetrexed and Platinum Chemotherapy to Treat Malignant Pleural Mesothelioma (MPM)

Read More: Merck                                                                                                   

Glycomine’s GLM101 Gains the US FDA’s Fast Track Designation to Treat Phosphomannomutase 2-Congenital Disorder of Glycosylation (PMM2-CDG)

Read More: Glycomine       

Novartis Reports the US FDA’s Approval of Kisqali (Ribociclib) for the Treatment of HR+/HER2- Early Breast Cancer

Read More: Novartis                                          

Johnson & Johnson Reports the US FDA’s Approval of Rybrevant Plus Standard of Care to Treat EGFR-Mutated NSCLC

Read More: Johnson & Johnson                                                                            

 

Mindpeak Partners with Roche to Strengthen Cancer Diagnostics Using AI

Read More: Mindpeak & Roche                                                                               

Astellas Reports the US FDA Listing of DIGITIVA to Manage Heart Failure

Read More: Astellas                                                                                       

 

Vivtex Partners with Equillium to Develop EQ302 for Gastrointestinal Inflammation

Read More: Vivtex & Equillium                                                                                

PharmaJet Join Forces with Scancell to Develop and Commercialize Needle-free DNA Vaccine for Advanced Melanoma

Read More: PharmaJet & Scancell                                                                          

 

Boston Scientific Reports the US FDA’s Expanded Approval of INGEVITY+ Pacing Leads for Conduction System Pacing

Read More: Boston Scientific                                                                                   

AngioDynamics Commences the RECOVER-AV Study of AlphaVac F1885 System to Treat Pulmonary Embolism

Read More: AngioDynamics                                                                                      

 

Organon to Acquire Dermavant for an Aggregate of ~$1.2B

Read More: Organon & Dermavant                                                                       

 

Accord BioPharma’s Hercessi 420mg (Biosimilar, Herceptin) Receives the US FDA’s Approval to Treat Various HER2-Overexpressing Cancer

Read More: Accord BioPharma                                                                                

 

Elanco Animal Health Reports the US FDA’s Approval of Zenrelia (Ilunocitinib) to Treat Canine Dermatological Disorders

Read More: Elanco                                                                                                  

epiq Animal Health and ArmOR Hand Gloves Collaborate to Offer Novel Products for Veterinarians within the Animal Health Distribution Channels

Read More: Epiq Animal Health                                                                                  

 

Rakuten Medical Highlights the Preclinical Results of RM-0256 at JCA 2024

Read More: Rakuten Medical                 

Related News: PharmaShots Weekly Snapshots (September 09 – September 13, 2024)                                                                 


Disha Nankani

Disha is a content writer at PharmaShots. She is passionate and curious about recent updates and developments in MedTech and Pharma industry. She covers news related to clinical trial results and updates. She can be contacted at connect@pharmashots.com.

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