Recent blog posts
Latigo Biotherapeutics Initiates Phase 1 Trial of LTG-305 for Non-Opioid Pain Management
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Latigo Biotherapeutics Initiates Phase 1 Trial of LTG-305 for Non-Opioid Pain Management
22 October 2024
Latigo Biotherapeutics has administered the first dose to a participant in its Phase 1 clinical trial for LTG-305, aimed at non-opioid pain management.
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Dosing Begins in IgGenix’s Phase 1 “ACCELERATE Peanut” Trial for Peanut Allergies
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Dosing Begins in IgGenix’s Phase 1 “ACCELERATE Peanut” Trial for Peanut Allergies
18 October 2024
IgGenix has reported that the initial patient has been dosed in its Phase 1 trial, named "ACCELERATE Peanut," which is testing IGNX001 for peanut allergies.
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Innovent Announces Success of Phase 2 Trial for Picankibart (IBI112) in Chinese Ulcerative Colitis Patients
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Innovent Announces Success of Phase 2 Trial for Picankibart (IBI112) in Chinese Ulcerative Colitis Patients
18 October 2024
Innovent has revealed that its Phase 2 clinical trial of Picankibart (IBI112) in Chinese patients with ulcerative colitis has met its primary goal.
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Alnylam Submits Vutrisiran Application to EMA for ATTR Amyloidosis with Cardiomyopathy
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Alnylam Submits Vutrisiran Application to EMA for ATTR Amyloidosis with Cardiomyopathy
18 October 2024
Alnylam has filed a regulatory application with the European Medicines Agency for Vutrisiran aimed at treating ATTR amyloidosis with cardiomyopathy.
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SciRhom Begins Administering Doses in First Human Trial for Its Main Development Project SR-878
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SciRhom Begins Administering Doses in First Human Trial for Its Main Development Project SR-878
18 October 2024
SciRhom GmbH has announced the initiation of participant dosing in their first clinical trial for the advanced development program SR-878.
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UroGen has announced that the FDA has accepted its new drug application for UGN-102
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UroGen has announced that the FDA has accepted its new drug application for UGN-102
18 October 2024
UroGen Pharma announced the acceptance of its NDA by the U.S. FDA for the investigational product UGN-102 (mitomycin) intended for intravesical administration.
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FDA Approves Adicet Bio's IND Amendment for ADI-001 Studies in Idiopathic Inflammatory Myopathy and Stiff Person Syndrome
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FDA Approves Adicet Bio's IND Amendment for ADI-001 Studies in Idiopathic Inflammatory Myopathy and Stiff Person Syndrome
18 October 2024
Adicet Bio has received FDA approval for an IND amendment to study ADI-001 in idiopathic inflammatory myopathy and Stiff Person Syndrome.
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Apretude (Cabotegravir) Shows Over 99% Effectiveness in Real-World Studies, Reports ViiV Healthcare
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Apretude (Cabotegravir) Shows Over 99% Effectiveness in Real-World Studies, Reports ViiV Healthcare
18 October 2024
ViiV Healthcare reports over 99% effectiveness for Apretude (Cabotegravir Long-Acting) in real-world studies.
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Sanofi and Orano collaborate to create advanced radioligand therapies
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Sanofi and Orano collaborate to create advanced radioligand therapies
18 October 2024
Sanofi has partnered with Orano Med, a branch of the Orano Group that leads in the advancement of targeted alpha therapies for cancer treatment.
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uniQure Begins First Patient Treatment in Phase I/II Trial of AMT-162 for SOD1-ALS
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uniQure Begins First Patient Treatment in Phase I/II Trial of AMT-162 for SOD1-ALS
17 October 2024
uniQure N.V. has announced that the initial participant has received a dose in the Phase I/II clinical study of AMT-162.
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Three Gan & Lee Pharmaceuticals Drugs, GZR18, GZR4, and GZR101, Succeed in Phase 2 Trials
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Three Gan & Lee Pharmaceuticals Drugs, GZR18, GZR4, and GZR101, Succeed in Phase 2 Trials
17 October 2024
Three novel drugs by Gan & Lee Pharmaceuticals-GZR18, GZR4, and GZR101 injections-meet primary goals in Phase 2 trials.
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Amgen Reports Positive Phase 3 Outcomes for Uplizna® in Generalized Myasthenia Gravis at AANEM 2024
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Amgen Reports Positive Phase 3 Outcomes for Uplizna® in Generalized Myasthenia Gravis at AANEM 2024
17 October 2024
Amgen reveals favorable Phase 3 results for Uplizna® (inebilizumab-cdon) in treating generalized myasthenia gravis at AANEM 2024.
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