Recent blog posts
LIB Therapeutics Reveals Positive Phase 3 Lerodalcibep Data at EAS Congress
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LIB Therapeutics Reveals Positive Phase 3 Lerodalcibep Data at EAS Congress
3 June 2024
LIB Therapeutics Shares Positive Phase 3 Lerodalcibep Results at 92nd European Atherosclerosis Society Congress.
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Atara Biotherapeutics Presents Early CAR T Therapy Research on CD19 at ISCT 2024
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Atara Biotherapeutics Presents Early CAR T Therapy Research on CD19 at ISCT 2024
3 June 2024
Atara Biotherapeutics Presents Early Research on ATA3219, a CAR T Therapy Targeting CD19 for B-Cell Autoimmune Diseases, at ISCT 2024.
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Bio-Thera and STADA Sign Exclusive Deal for Golimumab Biosimilar in Europe and UK
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Bio-Thera and STADA Sign Exclusive Deal for Golimumab Biosimilar in Europe and UK
3 June 2024
The partnership involves the commercialization and licensing of BAT2506, a biosimilar of Simponi® (golimumab).
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Outlook Therapeutics Gains EU Approval for Wet AMD Drug LYTENAVA™
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Outlook Therapeutics Gains EU Approval for Wet AMD Drug LYTENAVA™
31 May 2024
Outlook Therapeutics® Gains European Commission Approval for Marketing LYTENAVA™ (bevacizumab gamma) to Treat Wet AMD.
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FDA Grants Approval for First Interchangeable Biosimilar to Treat Two Uncommon Conditions
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FDA Grants Approval for First Interchangeable Biosimilar to Treat Two Uncommon Conditions
31 May 2024
The U.S. Food and Drug Administration has granted approval to Bkemv (eculizumab-aeeb) as the first interchangeable biosimilar to Soliris (eculizumab) for the treatment of specific rare conditions.
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TROPION-Lung01 Trial: Datopotamab Deruxtecan Improves Survival in Advanced Non-Small Cell Lung Cancer
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TROPION-Lung01 Trial: Datopotamab Deruxtecan Improves Survival in Advanced Non-Small Cell Lung Cancer
31 May 2024
In the TROPION-Lung01 Phase III trial, datopotamab deruxtecan significantly improved overall survival compared to chemotherapy in patients with advanced nonsquamous non-small cell lung cancer.
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FDA Grants Priority Review to Sarclisa for Newly Diagnosed Multiple Myeloma Patients Ineligible for Transplant
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FDA Grants Priority Review to Sarclisa for Newly Diagnosed Multiple Myeloma Patients Ineligible for Transplant
31 May 2024
Sarclisa received FDA priority review for treating newly diagnosed multiple myeloma patients ineligible for transplant.
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TILT Biotherapeutics Shares Clinical Results of TILT-123 for Ovarian Cancer at ASCO 2024
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TILT Biotherapeutics Shares Clinical Results of TILT-123 for Ovarian Cancer at ASCO 2024
30 May 2024
TILT Biotherapeutics' one abstract highlights encouraging safety and efficacy findings of TILT-123 in patients with ovarian cancer.
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selectION Announces Phase 1b Trial Start for si-544 in Psoriasis Vulgaris and Psoriatic Arthritis Patients
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selectION Announces Phase 1b Trial Start for si-544 in Psoriasis Vulgaris and Psoriatic Arthritis Patients
30 May 2024
selectION, Inc. declared the commencement of a Phase 1b study involving its leading candidate si-544 in adult individuals suffering from psoriasis vulgaris or psoriatic arthritis.
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REGN7075 Bispecific Antibody Shows Anti-Tumor Effects with Libtayo, Findings at ASCO
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REGN7075 Bispecific Antibody Shows Anti-Tumor Effects with Libtayo, Findings at ASCO
29 May 2024
Novel Bispecific Antibody REGN7075 (EGFRxCD28) Shows Anti-Tumor Effects with Libtayo® (cemiplimab); Findings to be Presented at ASCO.
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I-Mab Unveils Promising Phase 1 Results for Ragistomig at ASCO 2024
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I-Mab Unveils Promising Phase 1 Results for Ragistomig at ASCO 2024
29 May 2024
I-Mab Releases Promising Phase 1 Results for PD-L1x4-1BB Bispecific Antibody Ragistomig at ASCO 2024.
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BioAtla to Present Promising Phase 1 Evalstotug Trial Results at 2024 ASCO Conference
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BioAtla to Present Promising Phase 1 Evalstotug Trial Results at 2024 ASCO Conference
29 May 2024
BioAtla to Showcase Phase 1 Evalstotug Clinical Trial Outcomes Highlighting Clinical Benefits at the 2024 ASCO Annual Conference.
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