Recent blog posts
Sensei Biotherapeutics Shares Encouraging Phase 1 Dose Escalation Study Results for SNS-101
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Sensei Biotherapeutics Shares Encouraging Phase 1 Dose Escalation Study Results for SNS-101
29 May 2024
Sensei Biotherapeutics, Inc. has announced promising clinical results from the dose-escalation segment of its Phase 1/2 study on SNS-101.
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Coherus Reveals Initial Findings from Phase I Dose-escalation Trial of its CCR8-targeting Antibody, CHS-114
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Coherus Reveals Initial Findings from Phase I Dose-escalation Trial of its CCR8-targeting Antibody, CHS-114
29 May 2024
Coherus BioSciences, Inc. presented results from the CHS-114 monotherapy dose escalation part of its Phase 1 trial at the ASCO Annual Meeting.
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Cure Genetics Unveils Positive Safety and Efficacy of CAR-NKT Therapy CGC729 in RCC at ASGCT 2024
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Cure Genetics Unveils Positive Safety and Efficacy of CAR-NKT Therapy CGC729 in RCC at ASGCT 2024
29 May 2024
Cure Genetics Revealed Positive Safety and Effectiveness Data for CAR-NKT Treatment CGC729 in RCC at ASGCT 2024.
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Abdera Therapeutics Receives FDA Approval for IND Application of ABD-147
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Abdera Therapeutics Receives FDA Approval for IND Application of ABD-147
29 May 2024
Abdera Therapeutics Inc. has revealed that the U.S. Food and Drug Administration has approved their Investigational New Drug application for ABD-147.
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Aulos Bioscience Shares Favorable Preliminary Phase 1/2 Data for AU-007 at 2024 ASCO Meeting
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Aulos Bioscience Shares Favorable Preliminary Phase 1/2 Data for AU-007 at 2024 ASCO Meeting
29 May 2024
Aulos Bioscience revealed preliminary outcomes from its Phase 1/2 study of AU-007.
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European Commission Approves Celltrion's Omlyclo®, First Omalizumab Biosimilar in Europe
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European Commission Approves Celltrion's Omlyclo®, First Omalizumab Biosimilar in Europe
29 May 2024
Celltrion gains European Commission approval for Omlyclo® (CT-P39), the first omalizumab biosimilar sanctioned in Europe.
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EMA Approves Henlius and Organon's Biosimilar HLX14 for Prolia® and Xgeva®
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EMA Approves Henlius and Organon's Biosimilar HLX14 for Prolia® and Xgeva®
28 May 2024
The European Medicines Agency (EMA) has approved the filings by Henlius and Organon for their biosimilar candidate HLX14 to Prolia® and Xgeva® (denosumab).
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Kymera Therapeutics Reveals New Preclinical Data for KT-621, an Oral STAT6 Degrader, at ATS Conference
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Kymera Therapeutics Reveals New Preclinical Data for KT-621, an Oral STAT6 Degrader, at ATS Conference
28 May 2024
Kymera Therapeutics Unveils Novel Preclinical Findings for KT-621, an Oral STAT6 Degrader, at ATS Conference.
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Scholar Rock Launches Phase 2 Apitegromab Trial and Unveils New SRK-439 Preclinical Obesity Data
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Scholar Rock Launches Phase 2 Apitegromab Trial and Unveils New SRK-439 Preclinical Obesity Data
28 May 2024
Scholar Rock begins Phase 2 EMBRAZE trial for Apitegromab and reveals new preclinical results for SRK-439 in treating obesity.
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Zai Lab Starts Worldwide Phase 2 Study Testing ZL-1102 for Treating Chronic Plaque Psoriasis Topically
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Zai Lab Starts Worldwide Phase 2 Study Testing ZL-1102 for Treating Chronic Plaque Psoriasis Topically
28 May 2024
Zai Lab Limited announced the dosing of the first participant in a global Phase 2 trial of its anti-IL-17 treatment, ZL-1102, for chronic plaque psoriasis.
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Dyne Therapeutics Unveils Positive ACHIEVE and DELIVER Study Results for DYNE-101 in DM1 and DYNE-251 in DMD
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Dyne Therapeutics Unveils Positive ACHIEVE and DELIVER Study Results for DYNE-101 in DM1 and DYNE-251 in DMD
28 May 2024
Dyne Therapeutics Reveals Latest Clinical Results from ACHIEVE Study of DYNE-101 in DM1 and DELIVER Study of DYNE-251 in DMD Highlighting Significant Effects on Key Disease Indicators and Improvements in Several Functional Outcomes.
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Rapid-Acting Insulin AT278 Proves Superior in Phase I Trial for Overweight Type 2 Diabetics
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Rapid-Acting Insulin AT278 Proves Superior in Phase I Trial for Overweight Type 2 Diabetics
28 May 2024
AT278 Ultra-Concentrated Rapid-Acting Insulin Shows Superiority in Phase I Trial for Overweight and Obese Type 2 Diabetics.
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