AGAMREE® is approved by MHRA for treating Duchenne muscular dystrophy (DMD) in patients 4 years of age and older in UK January 14, 2025 – Santhera Pharmaceuticals (SIX: SANN) announces that the Scottish Medicines Consortium (SMC) has published recommendations that AGAMREE® (vamorolone) is accepted for use within NHS Scotland for the treatment of Duchenne muscular dystrophy (DMD) in patients 4 years of age and older. Dario Eklund, CEO of Santhera, commented: "I am delighted that the team has sec

— Indication expands to include treatment-naïve patients — — The 2021 conditional approval in previously treated patients converted to full approval — Jan. 14, 2025 -- HUTCHMED (China) Limited (“HUTCHMED”) (Nasdaq/AIM:​HCM; HKEX:​13) today announces that the supplemental New Drug Application for ORPATHYS® (savolitinib) has been granted approval by the China National Medical Products Administration (“NMPA”) for the treatment of adult patients with locally advanced or metastatic non-small cell lu

Jan. 13, 2025 -- genXtraits Inc. (genXtraits) and Solis Agrosciences Inc. (Solis) today announced that they have entered into an agreement under which Solis will conduct certain R&D services for genXtraits to accelerate the genXtraits’ novel crop variety development programs. genXtraits is an innovative biotech start-up, which is developing new crop varieties that carry valuable traits such as environmental stress tolerance and improved nutritional composition. The company has a proprietary bi

Jan. 14, 2025 -- PulseSight Therapeutics SAS, an ophthalmology biotech company developing disruptive non-viral vectorized therapies with minimally-invasive delivery technology, today announces it has submitted a Clinical Trial Authorization (CTA) to Agence Nationale de Sécurité du Médicament et des produits de santé (ANSM) for a Phase I trial (PST-611-CT1) assessing the safety and tolerability of PST-611 in humans. PST-611-CT1 is a first-in-human single ascending dose trial aiming to confirm t

Jan. 13, 2025 -- Corvus Pharmaceuticals, Inc. (NASDAQ: CRVS), a clinical-stage biopharmaceutical company, today announced new interim data from the randomized, double-blind, placebo-controlled Phase 1 clinical trial evaluating soquelitinib in patients with moderate to severe atopic dermatitis. The data, which include previously reported results from cohort 1 of the trial and new data covering 10 patients with 28-day follow-up from cohort 2 of the trial, demonstrated a favorable safety profile

Study conducted under the CRADA agreement between NCI and Oryzon Jan. 13, 2025 - Oryzon Genomics, S.A. (ISIN Code: ES0167733015, ORY), a clinical-stage biopharmaceutical company leveraging epigenetics to develop therapies in diseases with strong unmet medical need, announced today that the first patient has been dosed in a Phase I dose-finding clinical trial of iadademstat, Oryzon’s potent and selective LSD1 inhibitor, in combination with venetoclax and azacitidine in newly diagnosed acute myel

KRRO-110 is the first product candidate from Korro’s proprietary RNA editing OPERATM platform Interim readout from REWRITE expected in the second half of 2025 Korro to advance additional pipeline programs towards clinical development Jan. 13, 2025 -- Korro Bio, Inc. (Korro) (Nasdaq: KRRO), a clinical-stage biopharmaceutical company focused on developing a new class of genetic medicines based on editing RNA for both rare and highly prevalent diseases, today announced the initiation of dosing in

-- One year after the second vaccine dose, the anti-gE antibody immune response to amezosvatein continues to be non-inferior to Shingrix Jan. 12, 2025 -- Curevo Vaccine (Curevo), a privately-held clinical-stage biotechnology company dedicated to developing varicella zoster virus (VZV) vaccines with improved tolerability and accessibility, today announced positive updated immunogenicity and safety data from its 876-patient Phase 2 trial of amezosvatein (a non-mRNA, adjuvanted subunit vaccine als

Jan. 10, 2025 -- InflammX Therapeutics Inc., a clinical-stage biotechnology company focused on developing innovative therapies for retinal diseases with significant unmet needs, announced today that it has entered into an option agreement granting leading global eye health company Bausch + Lomb the right to acquire the company. This strategic move aligns with a shared goal of advancing groundbreaking treatments addressing unmet medical needs in ophthalmology. InflammX’s pipeline includes a cutt

2025年1月13日，复宏汉霖（2696.HK）宣布与Abbott签署许可协议，授予其在69个新兴市场国家和地区独家或半独家开发和商业化公司自主开发的四款生物类似药和一款生物创新药，协议覆盖亚洲、拉丁美洲和加勒比海地区及中东北非。该许可协议是在双方现有肿瘤领域生物类似药合作的基础上进一步深化。 根据新协议，预计到2027年，第一批分子候选物将上市，其余产品待完成临床开发和注册。Abbott将负责合作区域内合作产品的上市注册，并撬动其现有业务的广泛影响力和行业领导地位来推动合作产品的市场推广。作为一家专注于肿瘤、自身免疫疾病及眼科疾病的国际化生物制药公司，复宏汉霖将于其位于上海的GMP认证生产基地生产这些药物。 此次双方扩大合作，致力于令全球患者获得高质量、可负担的先进生物药，进一步兑现双方在新兴市场提供更多先进治疗选择的承诺。 复宏汉霖很高兴能与Abbott进一步加深合作。Abbott凭借其值得信赖的优质成熟药品、持续的技术创新能力以及完备的本地分销网络，于新兴市场达成稳健增长，已然成为新兴市场医疗领域的领军企业。此次双方再度携手，有力彰显了双方致力于推动全球健康可及性这一共同愿