Mineralys Therapeutics Announces First Patient Dosed in the ADVANCE-HTN Pivotal Trial of Lorundrostat for the Treatment of Uncontrolled and Resistant Hypertension

por Ysios Capital

Mineralys Therapeutics today announced the first patient dosed in the ADVANCE-HTN pivotal trial to evaluate the safety and efficacy of lorundrostat for the treatment of uncontrolled hypertension (uHTN...

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SparingVision Presents Progress of its Lead Gene Therapy Program SPVN06 at ARVO 2023

por Ysios Capital

SparingVision, a clinical-stage genomic medicine company developing vision-saving treatments for ocular diseases, shares progress in its lead gene therapy program, SPVN06, and research on retinitis pi...

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Minoryx presents positive interim results from NEXUS registration study for leriglitazone targeting pediatric ALD patients with cerebral adrenoleukodystrophy (cALD)

por Ysios Capital

Minoryx Therapeutics today announces 24-week interim results from NEXUS. This open label registration-enabling clinical trial is assessing the safety and efficacy of lead candidate leriglitazone, a no...

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Kala Pharmaceuticals Receives FDA Fast Track Designation for KPI-012, a Human MSC-S Therapy for Persistent Corneal Epithelial Defect

por Ysios Capital

Kala Pharmaceuticals today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for Kala’s human mesenchymal stem cell secretome (MSC-S) therapy (KPI-012) fo...

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Kala Pharmaceuticals Announces Positive Safety Update from Cohort 1 of CHASE Phase 2b Clinical Trial Evaluating KPI-012 in Patients with PCED

por Ysios Capital

Kala Pharmaceuticals today announced positive safety data from the first cohort of the CHASE (Corneal Healing After SEcretome therapy) Phase 2b clinical trial evaluating KPI-012, a human mesenchymal s...

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Mineralys Therapeutics Reports Fourth Quarter and Full Year 2022 Financial Results and Provides Corporate Update

por Ysios Capital

Mineralys Therapeutics, Inc. (Nasdaq: MLYS), a clinical-stage biopharmaceutical company focused on developing medicines to target diseases driven by abnormally elevated aldosterone, today announced fi...

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Am-Pharma to present data from phase 3 revival study at upcoming scientific conferences

por Ysios Capital

AM-Pharma B.V. today announced that Professor Peter Pickkers, M.D., Ph.D., principal investigator of the Phase 3 REVIVAL study, will present data from the study at two upcoming scientific conferences....

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AELIX Therapeutics presenta resultados positivos del ensayo clínico de fase IIa aleatorizado y controlado con placebo de su vacuna terapéutica contra el VIH en combinación con un inmunomodulador

por Ysios Capital

El estudio evaluó la seguridad, tolerabilidad, inmunogenicidad y eficacia de la vacuna terapéutica contra el VIH de células T HTI de AELIX en combinación con el agonista del receptor Toll-Like 7 (...

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NorthSea Therapeutics provides clinical update reflecting progress across NASH and metabolic disorders programmes

por Ysios Capital

NorthSea Therapeutics today provides an update on its clinical pipeline of structurally engineered fatty acids (‘SEFAs’), a new class of fatty acids drugs, for the treatment of non-alcoholic st...

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SparingVision’s lead asset SPVN06 clears IND application in the US for the treatment of retinitis pigmentosa

por Ysios Capital

PRODYGY is a Phase I/II study to assess the safety, tolerability, efficacy and quality of life following a single subretinal injection of SPVN06 in the worst-seeing eye of adult patients with RP due t...

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SpliceBio, participada por Ysios y Asabys, recibe el premio a la 'Serie A del año' en los European Lifestars awards

por Ysios Capital

SpliceBio, compañía biotecnológica de terapia génica con sede en Barcelona basada en tecnología desarrollada en la Universidad de Princeton, ha recibido el galardón a la “Ronda de Inversión S...

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Xeltis starts pivotal clinical trial with first ever restorative synthetic hemodialysis access graft

por Ysios Capital

The AXESS European pivotal trial is a prospective, single arm study to evaluate the safety and performance of aXess in patients with end-stage renal disease who need hemodialysis.

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