Recent blog posts
ProMIS Neurosciences begins Phase 1a trial, administering PMN310, a potential Alzheimer's treatment, to initial participants
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ProMIS Neurosciences begins Phase 1a trial, administering PMN310, a potential Alzheimer's treatment, to initial participants
29 November 2023
ProMIS Neurosciences initiates Phase 1a clinical trial, injecting the first participants with PMN310, a potential Alzheimer’s Disease treatment.
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Immix Biopharma's IND for CAR-T NXC-201 approved by FDA, enabling treatment for U.S. patients
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Immix Biopharma's IND for CAR-T NXC-201 approved by FDA, enabling treatment for U.S. patients
29 November 2023
Immix Biopharma confirms IND application for CAR-T NXC-201 has been sanctioned by FDA, allowing treatment dosage for U.S. patients.
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Omnix Medical gets green light from U.S. FDA for Phase II testing of its advanced anti-infective agent OMN6
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Omnix Medical gets green light from U.S. FDA for Phase II testing of its advanced anti-infective agent OMN6
28 November 2023
The biopharmaceutical company Omnix Medical, known for creating advanced anti-infectives to combat serious infections, has reported today that their upcoming Phase II trial for their innovative anti-infective, OMN6, has received approval from the FDA.
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The OCEANIC-AF research was prematurely terminated due to insufficient effectiveness
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The OCEANIC-AF research was prematurely terminated due to insufficient effectiveness
28 November 2023
The OCEANIC-AF phase III trial comparing asundexian and apixaban in stroke-risk atrial fibrillation patients will end early. This is based on the Independent Data Monitoring Committee's recommendation, as asundexian showed lower efficacy than the control. Bayer will analyze the data further and share the results later.
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Vigil Neuroscience: Phase 2 IGNITE trial shows promising early results for Iluzanebart (VGL101) in treating ALSP
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Vigil Neuroscience: Phase 2 IGNITE trial shows promising early results for Iluzanebart (VGL101) in treating ALSP
28 November 2023
Vigil Neuroscience has revealed encouraging initial results from the Phase 2 IGNITE clinical trial. This trial aims to test the potential of Iluzanebart (VGL101) in treating ALSP.
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AskBio begins Phase 1 trial with first patient for their MSA-P gene therapy, AB-1005
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AskBio begins Phase 1 trial with first patient for their MSA-P gene therapy, AB-1005
28 November 2023
AskBio reveals the enrollment of their initial patient into the Phase 1 trial for AB-1005 (AAV2-GDNF), their gene therapy solution to Multiple System Atrophy-Parkinsonian Type (MSA-P).
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Medicenna unveils positive survival results from the Phase 2b trial of Bizaxofusp for recurrent Glioblastoma at the 28th annual NeuroOncology Society meeting
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Medicenna unveils positive survival results from the Phase 2b trial of Bizaxofusp for recurrent Glioblastoma at the 28th annual NeuroOncology Society meeting
24 November 2023
Medicenna reports promising survival gains from the Phase 2b trial of Bizaxofusp for relapsed Glioblastoma, revealed at the 28th yearly NeuroOncology Society gathering.
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EBGLYSS® (lebrikizumab) received European Commission approval for treating moderate-to-severe atopic dermatitis
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EBGLYSS® (lebrikizumab) received European Commission approval for treating moderate-to-severe atopic dermatitis
24 November 2023
EBGLYSS® (lebrikizumab), developed by Almirall, has been given the green light by the European Commission for the treatment of moderate-to-severe atopic dermatitis.
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US approved Truqap (capivasertib) and Faslodex combo for advanced HR-positive breast cancer
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US approved Truqap (capivasertib) and Faslodex combo for advanced HR-positive breast cancer
24 November 2023
US approval granted for combination of Truqap (capivasertib) and Faslodex for treating advanced HR-positive breast cancer patients.
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Polaris Group begins phased BLA submission for ADI-PEG 20 to the U.S. FDA for Malignant Pleural Mesothelioma management
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Polaris Group begins phased BLA submission for ADI-PEG 20 to the U.S. FDA for Malignant Pleural Mesothelioma management
24 November 2023
Polaris Group commences phased submission of a BLA for ADI-PEG 20 to the U.S. FDA to manage Malignant Pleural Mesothelioma.
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FDA approves XTANDI® for advanced prostate cancer treatment
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FDA approves XTANDI® for advanced prostate cancer treatment
24 November 2023
Astellas and Pfizer's XTANDI® gets FDA approval for update, following fast-tracked review and EMBARK study results.
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Q32 Bio retrieves global rights for Bempikibart (ADX-914) back from Amgen
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Q32 Bio retrieves global rights for Bempikibart (ADX-914) back from Amgen
24 November 2023
Q32 Bio, a biotech company in clinical phase, is regaining full rights for bempikibart (formerly ADX-914) from Amgen to focus on developing immune-balancing biologic therapies.
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