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USD 44 Bn Medical Foods Market to Grow at a CAGR of 7.5% During 2023 to 2031 | Transparency Market Research
March 29, 2023 15:30 ET | Transparency Market Research
Wilmington, Delaware, United States, March 30, 2023 (GLOBE NEWSWIRE) -- According to market research conducted by TMR, the global medical foods industry was valued at USD 23.0 Bn in 2022 and is...
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AB2 Bio Completes Enrolment in Pivotal Phase 3 Trial of Tadekinig alfa to Treat Primary Monogenic IL-18 Driven HLH
March 07, 2023 03:00 ET | AB2 Bio Ltd
Topline pivotal Phase 3 results expected during second half of 2023Potential new treatment option in ultra-rare, life-threatening, primarily pediatric disease with no approved therapies Lausanne...
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Anti-Properdin Antibody (NM3086) Demonstrates Efficacy in a Primate Model of Wet-AMD and Dry-AMD
March 06, 2023 08:30 ET | Novelmed Therapeutics Inc
---Single therapy for multiple forms of Age-Related Macular Degeneration (AMD) NM3086 is a highly potent Alternative Pathway (AP) blocker that does not affect the Classical Pathway (CP).Dysfunction...
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Anti-Bb Antibody (NM8074) Receives US FDA Clearance to Start Clinical Trial in Naïve aHUS Patients (Rare Disease)
January 30, 2023 08:30 ET | Novelmed Therapeutics Inc
-- FDA Clears Initiation of Efficacy Trial in aHUS (Atypical Hemolytic Uremic Syndrome) Patients An Efficacy Trial in Adult aHUS Patients Who Are Naïve to Complement Inhibitor Therapy...
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Dutch biotech Xinvento raises seed round to develop a treatment for the rare disease Congenital Hyperinsulinism
April 21, 2022 02:00 ET | Xinvento BV
AMSTERDAM, April 21, 2022 (GLOBE NEWSWIRE) -- Xinvento, a biotech company aiming to improve the lives of those with Congenital Hyperinsulinism, announces today the completion of a seed funding...
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Amydis Announces Successful Completion of a Pre-IND Meeting with the FDA for the Development of a First-in-Class Retinal Tracer Targeting TDP43 for the Diagnosis of ALS
December 06, 2021 07:00 ET | Amydis, Inc.
SAN DIEGO, Dec. 06, 2021 (GLOBE NEWSWIRE) -- Amydis Inc., a biotechnology company developing novel ocular contrast agents (“tracers”) targeting CNS biomarkers in the eye, today announced the...
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Industry leaders seek to advance innovative resources for rare and orphan disease communities amid COVID-19 outbreak
April 27, 2020 13:00 ET | FFF Enterprises.com
Temecula, April 27, 2020 (GLOBE NEWSWIRE) -- FFF Enterprises and BioNews announced today that both rare and orphan disease advocates are joining forces to provide patients with resources to help...
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AB Science annonce que la FDA autorise le recrutement de patients aux USA dans l’étude de phase 3 du masitinib dans la Sclérose Latérale Amyotrophique (SLA)
March 31, 2020 11:35 ET | AB Science
Paris, 31 mars 2020, 17h30 La FDA autorise le recrutement de patients aux USA dans l’étude dephase 3 du masitinib dans la Sclérose Latérale Amyotrophique (SLA) AB Science SA (NYSE Euronext –...
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AB Science announces that FDA clears masitinib IND in Amyotrophic Lateral Sclerosis (ALS), allowing U.S. patient enrollment to commence in Phase 3 study
March 31, 2020 11:35 ET | AB Science
Paris, March 31, 2020, 5.30pm FDA clears masitinib IND in Amyotrophic Lateral Sclerosis (ALS), allowing U.S. patient enrollment to commence in Phase 3 study AB Science SA (NYSE Euronext -...
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AB Science announces the publication of new results in the peer-reviewed journal Glia that further support masitinib’s potential mode of action in ALS
December 23, 2019 02:11 ET | AB Science
Paris, 23 December 2019, 8.15am New results published in the peer-reviewed journal Gliafurther support masitinib’s potential mode of action in ALS AB Science SA (NYSE Euronext - FR0010557264 - AB)...