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| May 5, 2025 | OSE Immunotherapeutics Announces >90% of Responders Maintained Symptomatic Remission Through Extension Period on Lusvertikimab | OSE Immunotherapeutics Announces >90% of Responders Maintained Symptomatic Remission Through Extension Period on Lusvertikimab
Lusvertikimab well tolerated over the 24-week additional treatment period.
Oral presentation at DDW 2025 of cl... |
| Apr 29, 2025 | Novadip releases five-year follow-up results for NVD003, regenerative treatment for severe bone non-union of lower limb | No refractures were reported during long-term follow-up at five years
At 24-months post-implantation, 89% of patients achieved bone union
Novadip plans market launch of NVD003 in 2027
Mont Saint-Guibert, Belgium, April 29, 2025 – Novadip Bi... |
| Mar 14, 2025 | Hansa Biopharma's Breakthrough in Kidney Transplantation: A New Hope for Highly Sensitized Patients | In the world of medicine, breakthroughs often feel like a distant star—visible, yet unreachable. However, Hansa Biopharma is changing that narrative for highly sensitized kidney transplant patients. The company recently announced the comple... |
| Mar 11, 2025 | Hansa Biopharma completes enrolment in European Phase 3 20-HMedIdeS-19 Post Authorization Efficacy and Safety study in highly sensitized kidney transplant patients | Hansa Biopharma completes enrolment in European Phase 3 20-HMedIdeS-19 Post Authorization Efficacy and Safety study in highly sensitized kidney transplant patients
Tue, Mar 11, 2025 14:35 CET Report this content
Lund, Sweden, 11 March 2025.... |
| Oct 17, 2024 | Telix Q3 2024 Business Update - Quarterly Revenue Exceeds AU$200M | MELBOURNE, Australia, Oct. 17, 2024 /PRNewswire/ -- Telix Pharmaceuticals Limited (ASX: TLX, Telix, the Company) today provides an update on its revenue and operational performance for the quarter ended 30 September 2024 (Q3 2024).
Revenue ... |
| Dec 20, 2023 | Sedana Medical files submission for paediatric indication | Sedana Medical files submission for paediatric indication
Wed, Dec 20, 2023 08:00 CET Report this content
Sedana Medical AB (publ) announces that the company has submitted a Type II variation with the aim of including the paediatric populat... |
| Nov 16, 2023 | Key results of Sedana Medical’s paediatric study IsoCOMFORT published | Key results of Sedana Medical’s paediatric study IsoCOMFORT published
Thu, Nov 16, 2023 08:00 CET Report this content
Sedana Medical AB (publ) today announces that the main results from the paediatric IsoCOMFORT study have been published in... |
| Jul 19, 2023 | First patient treated with imlifidase in an investigator-initiated Phase 2 study in ANCA-associated vasculitis | First patient treated with imlifidase in an investigator-initiated Phase 2 study in ANCA-associated vasculitis
Wed, Jul 19, 2023 08:00 CET Report this content
Lund, Sweden 19 July, 2023. Hansa Biopharma (“Hansa”), a pioneer in enzyme techno... |
| Apr 18, 2023 | Nordic Nanovector Publishes Data from the PARADIGME Phase 2 Clinical Trials with Betalutin® on European Clinical Trials Database | Nordic Nanovector Publishes Data from the PARADIGME Phase 2 Clinical Trials with Betalutin® on European Clinical Trials Database
Tue, Apr 18, 2023 11:15 CET Report this content
Oslo, Norway,18 April 2023
Nordic Nanovector ASA (OSE: NANOV) (... |
| Mar 29, 2023 | Hansa Biopharma announces positive reimbursement decision in Spain for Idefirix[®] (imlifidase) as desensitization treatment for highly sensitized patients in kidney transplantation | Hansa Biopharma announces positive reimbursement decision in Spain for Idefirix[®] (imlifidase) as desensitization treatment for highly sensitized patients in kidney transplantation
Wed, Mar 29, 2023 15:00 CET Report this content
Lund, Swed... |
| Jul 11, 2022 | Hansa Biopharma announces first patient treated in the post-authorization efficacy study (PAES) of Idefirix® (imlifidase) in highly sensitized kidney transplant patients | Hansa Biopharma announces first patient treated in the post-authorization efficacy study (PAES) of Idefirix® (imlifidase) in highly sensitized kidney transplant patients
Mon, Jul 11, 2022 08:00 CET Report this content The PAES is an open-la... |
| Mar 14, 2022 | Update on US review of Fasenra in nasal polyps | Update on US review of Fasenra in nasal polyps
Mon, Mar 14, 2022 08:00 CET Report this content
14 March 2022 07:00 GMT
Update on US regulatory review of Fasenra
in chronic rhinosinusitis with nasal polyps
The US Food and Drug Administration... |
| Feb 11, 2022 | EMA initiates safety review on JAK inhibitors; Galapagos woes continue as it terminates latest study | Following the FDA’s issuance of a safety warning regarding JAK inhibitors, the safety committee of the European Medicines Agency on Friday initiated a review of these treatments, which are used to treat several chron... |
| Feb 10, 2022 | BioGaia Pharma announces First Patient Enrolled in Phase I Clinical Study Evaluating BGP014 in mild to moderate ulcerative colitis (AUCH-1). | BioGaia Pharma received formal approval from relevant authorities to proceed with both of its planned clinical trials during summer 2021. Investigational Medical Products were delivered to sites Q4 2021 and screening began. The first patien... |
| Feb 10, 2022 | BioGaia Pharma announces First Patient Enrolled in Phase I Clinical Study Evaluating BGP014 in mild to moderate ulcerative colitis (AUCH-1). | BioGaia Pharma announces First Patient Enrolled in Phase I Clinical Study Evaluating BGP014 in mild to moderate ulcerative colitis (AUCH-1).
Thu, Feb 10, 2022 09:30 CET Report this content
BioGaia Pharma received formal approval from releva... |
| Jan 26, 2022 | BioGaia Pharma announces First Patient Enrolled in Phase II Clinical Study Evaluating BGP345A for the treatment of opioid induced constipation (OIC-1) | BioGaia Pharma announces First Patient Enrolled in Phase II Clinical Study Evaluating BGP345A for the treatment of opioid induced constipation (OIC-1) Wed, Jan 26, 2022 09:30 CET
BioGaia Pharma received formal approval from relevant authori... |
| Jan 26, 2022 | BioGaia Pharma announces First Patient Enrolled in Phase II Clinical Study Evaluating BGP345A for the treatment of opioid induced constipation (OIC-1) | BioGaia Pharma received formal approval from relevant authorities to proceed with both of its planned clinical trials during summer 2021. Investigational Medical Products were delivered to sites Q4 2021 and screening began. The first patien... |
| Dec 8, 2021 | Last-gasp gene therapy saved a Syrian refugee’s life. Five years later, the boy is thriving and a clinical trial is starting | In the summer of 2015, a 7-year-old named Hassan was admitted to the burn unit of the Ruhr University Children’s Hospital in Bochum, Germany, with red, oozing wounds from head to toe.
It wasn’t a fire that took his skin. It was a bacterial ... |
| Sep 10, 2021 | BioGaia : Pharma secures approval for two clinical trials for its pharmaceutical candidates | BioGaia Pharma has received formal approval from relevant authorities to proceed with both of its planned clinical trials. The trials are the next phase in the development of BioGaia Pharma's two pharmaceutical product candidates. The biolo... |
| Sep 10, 2021 | BioGaia Pharma secures approval for two clinical trials for its pharmaceutical candidates | BioGaia Pharma secures approval for two clinical trials for its pharmaceutical candidates Fri, Sep 10, 2021 10:00 CET
BioGaia Pharma has received formal approval from relevant authorities to proceed with both of its planned clinical trials.... |
| Jul 4, 2021 | Regulators in many European countries fail to ensure clinical trial data are available | Amid ongoing concerns over clinical trial transparency, a new report finds “notable gaps” in the quality and availability of clinical trial data in a European registry, pointing to inconsistent and often inadequate oversight by regulators i... |
| Apr 14, 2021 | Novel COVID-19 therapy enters phase 2 clinical trials | |
| Apr 14, 2021 | Novel COVID-19 therapy enters phase 2 clinical trials | Kinarus AG is a clinical-stage biopharmaceutical company focused on bringing novel treatments to patients suffering from viral, respiratory, and ophthalmic diseases. The company's unique and innovative combinatorial therapeutic candidate KI... |
| Oct 21, 2020 | The MOTIVATE US webinar series is about to start | |
| May 9, 2020 | A Coronavirus Vaccine is Coming, but When? | wp_booster error:
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| May 9, 2020 | A Coronavirus Vaccine is Coming, but When? | wp_booster error:
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| Apr 14, 2020 | Central, Searchable Repository for all COVID-19 Clinical Trials Launches | What You Need to Know:
– Inato unveils central, searchable repository for all COVID-19 clinical trials designed to support clinical researchers, physicians, and biopharma organizations.
– By centralizing all clinical studies being conducted... |
| Aug 21, 2018 | FDA accepts Alexion’s application for next-generation PNH drug | ALXN1210 is a long-acting medicine with the same target as Soliris (eculizumab), for which Alexion won FDA approval for reducing red blood cell destruction – also known as hemolysis – in PNH in 2007, but which must be dosed more frequently.... |
| Nov 3, 2016 | What clinical trial results? Now you can see who isn’t sharing their findings | The results for nearly half of all clinical trials conducted by big drug makers during the last decade have not been published, and one company — Ranbaxy Laboratories — has not published findings for any of the nearly three dozen trials con... |
| Jan 20, 2016 | French debacle renews concern about clinical trial secrecy
Clinical trial reporting lapses visualized | The death of a volunteer in a calamitous drug trial in France last week renewed concerns about the safety of early-stage human testing and the lack of a comprehensive public database that tracks the outcomes of such clinical trials.
The vic... |
| Feb 20, 2014 | Raising the veil on clinical trial data | By Tom Ulrich
Ed. note: This is the first in a two- part series on making clinical trial data more transparent.
2013 was the year when big data became, well, big. Everyone from investment companies to public utilities to security agencies –... |
| FDA accepts Alexion’s application for next-generation PNH drug | The Food and Drug Administration has accepted for priority review Alexion Pharmaceuticals’ new drug for a rare blood disorder.
The New Haven, Connecticut-based company said Monday that the FDA would review its application for ALXN1210, a C5... |