Recent blog posts
ILiAD Biotechnologies announces unique evidence of protection against B. pertussis infection in Phase 2b Human Challenge Trials with BPZE1 Vaccine
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ILiAD Biotechnologies announces unique evidence of protection against B. pertussis infection in Phase 2b Human Challenge Trials with BPZE1 Vaccine
8 September 2023
ILiAD Biotechnologies, LLC, a biotech firm in the clinical trial phase, which is spearheading the creation of an unparalleled, progressive pertussis vaccine, reports promising preliminary results from the CHAMPION-1 clinical trial.
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Novo Nordisk Expands Wegovy Rollout in Europe Amid Supply Chain Challenges
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Novo Nordisk Expands Wegovy Rollout in Europe Amid Supply Chain Challenges
7 September 2023
Novo Nordisk is vigorously pursuing the rollout of the obesity medication, Wegovy, across Europe, despite grappling with supply chain issues.
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Zenas BioPharma publicizes significant licensing and teamwork contract with Bristol Myers Squibb, aiming to market the innovative bi-functional antibody Obexelimab
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Zenas BioPharma publicizes significant licensing and teamwork contract with Bristol Myers Squibb, aiming to market the innovative bi-functional antibody Obexelimab
7 September 2023
Zenas BioPharma disclosed today their signing of a licensing and partnership contract with Bristol Myers Squibb Company.
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Genmab and Seagen report that TIVDAK® achieved its main objective of enhancing overall survival rates in patients suffering from recurrent or metastatic cervical cancer
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Genmab and Seagen report that TIVDAK® achieved its main objective of enhancing overall survival rates in patients suffering from recurrent or metastatic cervical cancer
7 September 2023
Genmab A/S and Seagen Inc.  revealed that its main objective of overall survival when TIVDAK®(tisotumab vedotin-tftv) was used in comparison to chemotherapy only.
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Viatris announced that the FDA has preliminarily approved the formulation of abacavir (ABC)/dolutigravir (DTG)/lamivudine (3TC) for children infected with HIV
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Viatris announced that the FDA has preliminarily approved the formulation of abacavir (ABC)/dolutigravir (DTG)/lamivudine (3TC) for children infected with HIV
7 September 2023
The multinational healthcare firm, Viatris Inc., has shared news of the tentative approval from FDA)for an abacavir 60 mg/dolutegravir 5 mg/lamivudine 30 mg oral suspension tablet New Drug Application .
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Beactica Therapeutics announces their choice of BEA-17 for the preclinical candidate status
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Beactica Therapeutics announces their choice of BEA-17 for the preclinical candidate status
7 September 2023
Swedish precision oncology firm, Beactica Therapeutics AB, has today unveiled BEA-17 as their chosen preclinical candidate within the LSD1 initiative
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ACM Biolabs Releases Encouraging Findings from a Phase I Study for SARS-CoV-2 Enhancer Vaccine ACM-001
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ACM Biolabs Releases Encouraging Findings from a Phase I Study for SARS-CoV-2 Enhancer Vaccine ACM-001
7 September 2023
ACM Biolabs has revealed encouraging preliminary findings from a Phase I evaluation of ACM-001, their inaugural clinical-stage development initiative.
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InvIOs starts a new clinical trial of innovative cell therapy APN401 for solid tumors
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InvIOs starts a new clinical trial of innovative cell therapy APN401 for solid tumors
7 September 2023
InvIOs GmbH revealed today that it has launched patient enrollment for a Phase 1b trial of its innovative autologous cell therapy, APN401, focusing on solid tumor patients.
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EU Commission Approves Pfizer's ABRYSVO™ for RSV Protection in Infants, Elderly via Maternal Vaccination
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EU Commission Approves Pfizer's ABRYSVO™ for RSV Protection in Infants, Elderly via Maternal Vaccination
6 September 2023
The European Union Commission has approved Pfizer's ABRYSVO™ to protect infants and the elderly from Respiratory Syncytial Virus infections via maternal vaccination.
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Rallybio Unveils Phase 1 Data for Single Ascending Dose of RLYB116, a Novel Subcutaneous Complement Component 5 Inhibitor
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Rallybio Unveils Phase 1 Data for Single Ascending Dose of RLYB116, a Novel Subcutaneous Complement Component 5 Inhibitor
6 September 2023
RLYB116, a potential long-acting solution, is a subcutaneously administered C5 inhibitor which is currently being developed for managing patients with complement-mediated diseases.
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Bayer has high expectations for Kerendia in treating heart failure
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Bayer has high expectations for Kerendia in treating heart failure
6 September 2023
Bayer’s Kerendia (finerenone)  had gained approval for usage in managing chronic kidney diseases affiliated with type 2 diabetes two summers ago.
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Stallerges Greer Announces Global Nestle Contract for Palforzia® Peanut Allergy Treatment
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Stallerges Greer Announces Global Nestle Contract for Palforzia® Peanut Allergy Treatment
6 September 2023
Stallerges Greer has disclosed a contract with Nestle regarding the use of Palforzia ® A global agreement to treat peanut allergies.
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