Recent blog posts
Electra Therapeutics unveils initial study results from their active Phase 1b trial of ELA026 designed to combat secondary HLH
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Electra Therapeutics unveils initial study results from their active Phase 1b trial of ELA026 designed to combat secondary HLH
18 December 2023
Electra Therapeutics unveils initial study results from their active Phase 1b trial of ELA026 designed to combat secondary HLH (hemophagocytic lymphohistiocytosis)
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Agenus is set to secure a $25 million achievement fee from BMS for their collaborative TIGIT-CD96 dual targeting project
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Agenus is set to secure a $25 million achievement fee from BMS for their collaborative TIGIT-CD96 dual targeting project
18 December 2023
Agenus Inc., an innovator in immune-modulatory cancer treatments, announced reaching its second milestone in the global licensing agreement with Bristol Myers Squibb for BMS-986442, a bispecific TIGIT antibody with improved Fc functionality.
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Atara Bio reveals promising initial findings for its off-the-shelf CAR therapy, ATA3431, targeting CD20 and CD19, at ASH's 65th session
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Atara Bio reveals promising initial findings for its off-the-shelf CAR therapy, ATA3431, targeting CD20 and CD19, at ASH's 65th session
18 December 2023
Atara Biotherapeutics Unveils Encouraging Early Research Results for ATA3431, an Innovative Off-the-Shelf CAR Therapy Aimed at CD20 and CD19, at the 65th Annual Session of ASH.
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FDA and EMA Acknowledge Marstacimab Filing for Hemophilia A and B Therapy
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FDA and EMA Acknowledge Marstacimab Filing for Hemophilia A and B Therapy
18 December 2023
The FDA has approved Pfizer’s review request for marstacimab, a hemophilia A/B treatment for non-inhibitor patients.
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SystImmune collaborates with Bristol Myers Squibb in a major worldwide partnership to advance and market BL-B01D1
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SystImmune collaborates with Bristol Myers Squibb in a major worldwide partnership to advance and market BL-B01D1
18 December 2023
SystImmune and industry giant Bristol Myers Squibb have announced a partnership and licensing agreement focused on BL-B01D1, SystImmune's cutting-edge EGFRxHER3 bispecific antibody-drug conjugate.
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Oculis Starts Phase 2b RELIEF Trial Enrolling First Patient for Licaminlimab (OCS-02), a Topical Anti-TNFα Drug for Dry Eye Treatment
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Oculis Starts Phase 2b RELIEF Trial Enrolling First Patient for Licaminlimab (OCS-02), a Topical Anti-TNFα Drug for Dry Eye Treatment
15 December 2023
Oculis Reveals Initial Participant Commencement in Phase 2b RELIEF Study for Topical Anti-TNFα Agent Licaminlimab (OCS-02) Aimed at Treating Dry Eye Conditions.
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Xilio Therapeutics Starts Phase 1 Trial Enrollment for XTX101 Combo and Updates Monotherapy Data
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Xilio Therapeutics Starts Phase 1 Trial Enrollment for XTX101 Combo and Updates Monotherapy Data
15 December 2023
Xilio Therapeutics Announces Initiation of Enrollment for Phase 1 Combination Trial of XTX101, a Tumor-Activated, Fc-Enhanced Anti-CTLA-4, and Updated Phase 1 Monotherapy Data.
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AltruBio Commences Initial Participant Recruitment for Second-Phase Clinical Trials of ALTB-268 Aimed at Managing Ulcerative Colitis
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AltruBio Commences Initial Participant Recruitment for Second-Phase Clinical Trials of ALTB-268 Aimed at Managing Ulcerative Colitis
15 December 2023
AltruBio Inc. starts Phase 2a trial for its drug ALTB-268 in ulcerative colitis patients with the first participant enrolled.
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Vittoria Biotherapeutics Announces FDA Clearance for VIPER-101 IND in T-Cell Lymphoma
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Vittoria Biotherapeutics Announces FDA Clearance for VIPER-101 IND in T-Cell Lymphoma
15 December 2023
Vittoria Biotherapeutics Reveals US FDA Approval of Investigational New Drug Submission for VIPER-101 to Address T-Cell Lymphoma Therapy.
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US Health Agency Endorses Bio-Thera's Avzivi® as Alternative to Avastin®, Authorizing Bevacizumab-tnjn Use
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US Health Agency Endorses Bio-Thera's Avzivi® as Alternative to Avastin®, Authorizing Bevacizumab-tnjn Use
15 December 2023
Bio-Thera Solutions, Ltd has made public the approval of their product Avzivi® (bevacizumab-tnjn) by the United States Food and Drug Administration.
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ExeGi Pharma Reveals Initiation of Participant Inclusion for EXE-346 in the PROF Study
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ExeGi Pharma Reveals Initiation of Participant Inclusion for EXE-346 in the PROF Study
15 December 2023
ExeGi Pharma, a biopharmaceutical pioneer in live biotherapeutics, has commenced patient enrollment for its pivotal PROF Trial to test EXE-346, a new treatment targeting frequent bowel movements post ileal pouch-anal anastomosis surgery.
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EU Authority Sanctions Pfizer's Treatment, ELREXFIO®, for Recurring Intractable Multiple Myeloma
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EU Authority Sanctions Pfizer's Treatment, ELREXFIO®, for Recurring Intractable Multiple Myeloma
15 December 2023
Pfizer Inc. has released an announcement that the European Commission has provided a conditional marketing approval for their product, ELREXFIO (elranatamab).
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