Recent blog posts
Hemab Therapeutics reveals promising early results for Glanzmann's Thrombasthenia drug, HMB-001, at 2024 EAHAD Congress
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Hemab Therapeutics reveals promising early results for Glanzmann's Thrombasthenia drug, HMB-001, at 2024 EAHAD Congress
19 February 2024
At the EAHAD Congress in 2024, Hemab Therapeutics Unveils Encouraging Initial Findings for Their Drug, HMB-001, Targeting Glanzmann's Thrombasthenia.
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China Grants First-Ever Approval to Crovalimab for Paroxysmal Nocturnal Hemoglobinuria (PNH) Therapy
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China Grants First-Ever Approval to Crovalimab for Paroxysmal Nocturnal Hemoglobinuria (PNH) Therapy
19 February 2024
Chugai Pharmaceutical announced that China's National Medical Products Administration approved its innovative C5 monoclonal antibody, crovalimab.
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In a Phase 2b trial, the oral peptide JNJ-2113 showed promise for moderate to severe psoriasis
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In a Phase 2b trial, the oral peptide JNJ-2113 showed promise for moderate to severe psoriasis
19 February 2024
In a Phase 2b clinical trial, the experimental oral peptide known as JNJ-2113 has shown encouraging outcomes for patients with moderate to severe psoriasis.
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REGENXBIO Hits Key Goal in RGX-121 Study for MPS II
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REGENXBIO Hits Key Goal in RGX-121 Study for MPS II
19 February 2024
REGENXBIO Confirms Major Milestone Reached in Crucial Study of RGX-121 as Therapy for MPS II, Successfully Hitting Primary Goal.
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Initial Human Participant Receives ZMA001 in Medical Study Targeting PAH Therapy
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Initial Human Participant Receives ZMA001 in Medical Study Targeting PAH Therapy
19 February 2024
Zymedi has begun first human trials of ZMA001, a novel monoclonal antibody for treating Pulmonary Arterial Hypertension.
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US FDA & Australian Health Authorities Approve ETX101, Encoded Therapeutics' Potential Genetic Treatment for Dravet Syndrome
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US FDA & Australian Health Authorities Approve ETX101, Encoded Therapeutics' Potential Genetic Treatment for Dravet Syndrome
18 February 2024
Encoded Therapeutics Reveals Approval from US FDA for IND Application and Consent from Australian Health Authorities for ETX101, a Genetic Treatment Prospect for Dravet Syndrome.
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Scholar Rock Unveils Initial Lab Results Indicating Advantages of SRK-439 in Supporting Weight Reduction
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Scholar Rock Unveils Initial Lab Results Indicating Advantages of SRK-439 in Supporting Weight Reduction
18 February 2024
Scholar Rock's Study Reveals SRK-439's Potential Influence on Muscle Mass and Metabolic Health in Weight Loss Efforts.
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Orchard Therapeutics Begins OTL-203 Study for Hurler's Syndrome in MPS-I
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Orchard Therapeutics Begins OTL-203 Study for Hurler's Syndrome in MPS-I
18 February 2024
Orchard Therapeutics Reveals Enrollment of Initial Participant in Key Study of OTL-203 Targeting Hurler's Syndrome in MPS-I.
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Positive Early Results of Rani Therapeutics' Phase 1 Trial for Oral RT-111
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Positive Early Results of Rani Therapeutics' Phase 1 Trial for Oral RT-111
18 February 2024
Rani Therapeutics Reports Encouraging Initial Outcomes from Phase 1 Trial of Oral RT-111, an Anti-IL-12/23 Antibody.
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Promising Early Results from Johnson & Johnson's Phase 3 & 2 Trials for Generalized Myasthenia Gravis and Sjögren's Disease Treatments
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Promising Early Results from Johnson & Johnson's Phase 3 & 2 Trials for Generalized Myasthenia Gravis and Sjögren's Disease Treatments
18 February 2024
Johnson & Johnson has announced encouraging initial findings from a critical Phase 3 trial with nipocalimab for treating generalized myasthenia gravis, as well as from a Phase 2 investigation in Sjögren's Disease.
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Technoderma's TDM-105795 Stage 2 Trial Shows Positive Hair Regrowth in Pattern Baldness
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Technoderma's TDM-105795 Stage 2 Trial Shows Positive Hair Regrowth in Pattern Baldness
18 February 2024
The Stage 2 trial for Technoderma's drug, TDM-105795, reveals positive outcomes for hair regeneration in individuals with pattern baldness.
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Sangamo Therapeutics Unveils Promising Phase 1/2 Results for Fabry Disease Research
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Sangamo Therapeutics Unveils Promising Phase 1/2 Results for Fabry Disease Research
18 February 2024
Sangamo Therapeutics Reveals New Findings from Phase 1/2 STAAR Research for Fabry Disease Indicating Continuous Efficacy and Unique Safety Data.
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