OxThera is a biopharmaceutical company with products in late stage clinical development focusing on Primary and Secondary Hyperoxaluria. OxThera’s intellectual property includes worldwide patents for compositions and treatment of hyperoxaluria with bacteria, and enzymes.

Primary hyperoxaluria type 1 : clinical, genetic and biochemical studies van Woerden provided by OxThera, Altus Pharmaceuticals, Ferring BV Hoofddorp,.

Primary hyperoxaluria is a rare autosomal recessive disorder leading to markedly elevated levels of endogenous oxalate i plasma and urine. High levels of oxalate cause kidney damage, including crystallization of oxalate in tissues and in the kidney. About OxThera OxThera AB is a Swedish biotech company developing a new treatment for primary hyperoxaluria (PH) - a rare genetic and devastating disease with fatal outcomes. Currently pharmaceutical treatment is not available and median age of death is 30, if patients are not transplanted. Our mission is to bring novel treatment options to rare kidney disease and to partner closely with the medical and patient communities we serve. Ultimately, our goal is to improve quality of life and to extend life expectancy of patients with primary hyperoxaluria.

Oxthera primary hyperoxaluria

APR 2009. LKP An Open Label (OL) Extension Study, 13 Nov 2017 OxThera is currently pursuing a complete Oxabact clinical development program for the treatment of patients suffering from Primary Hyperoxaluria 15 Apr 2020 Patients with primary hyperoxaluria (PH) often develop kidney stones and chronic OxThera, Inc. also provided partial funding for this study. 18 Jul 2019 The Primary Hyperoxaluria (Genito Urinary System And Sex Hormones) Dicerna Pharmaceuticals Inc; Intellia Therapeutics Inc; OxThera AB OxThera. Collaborator: FP7-SME-2013 Research for the benefit of SMEs program Primary Hyperoxaluria, Biological: Oxalobacter formigenes, Phase 2 PDF | On Jul 1, 2008, Christiaan van Woerden published Primary hyperoxaluria type 1 : clinical, genetic and biochemical studies | Find, read and cite all the OxThera AB is a Swedish biotech company developing a new treatment for primary hyperoxaluria (PH) - a rare genetic and de… See more. Headquarters. 2 Nov 2008 Primary hyperoxaluria type 1 (PH1) is a rare metabolic disorder OxThera.

2018-07-10

OxThera is a biopharmaceutical company with products in late stage clinical development focusing on Primary and Secondary Hyperoxaluria. OxThera’s intellectual property includes worldwide patents for compositions and treatment of hyperoxaluria with bacteria, and enzymes. /PRNewswire/ -- OxThera AB has been granted three Japanese patents during 2012 and 2013. The patents will secure the pharmaceutical composition and the method OxThera AB, a privately-held biopharmaceutical company dedicated to improving the lives of people with Primary Hyperoxaluri OxThera receives positive decision from EMA on Paediatric Investigational Plan (PIP) for treatment of primary hyperoxaluria with Oxalobacter formigenes | Placera OxThera AB, a Stockholm-based privately-held biopharmaceutical company, announced that the Phase 3 study with Oxabact ® in Primary Hyperoxaluria (PH) is now fully open for recruitment.

Primary hyperoxaluria is a rare autosomal recessive disorder leading to markedly elevated levels of endogenous oxalate i plasma and urine. High levels of oxalate cause kidney damage, including crystallization of oxalate in tissues and in the kidney.

39 likes. Welcome to OxThera’s page for our ePHex clinical trial!

Preclinical. (CDN). Invest. Stockholm. OxThera.
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2021-02-19 · Primary hyperoxaluria is a rare autosomal recessive inherited disorder of glyoxylate metabolism that causes an endogenous overproduction of oxalate. Oxalate cannot be degraded in humans and is mostly eliminated by the kidneys. The oxalate overproduction leads to kidney stones, nephrocalcinosis and kidney damage. OxThera AB, a Stockholm-based privately-held biopharmaceutical company, today announced that the Phase 3 study with Oxabact® in Primary Hyperoxaluria (PH) is now fully open for recruitment.

1 author BACKGROUND:In primary hyperoxaluria Type 1 (PH1), endogenous oxalate 1 Mar 2021 Abstract. Background In patients with primary hyperoxaluria (PH), endogenous oxalate OxThera Intellectual Property AB, Stockholm, Sweden. Health-Related Quality of Life (HRQoL) in Primary Hyperoxaluria (PH).
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Primary hyperoxaluria (PH) is a rare genetic metabolic disorder. There are three forms of PH (type 1, 2, and 3), caused by different enzyme deficiencies leading to excessive oxalate production. Oxalate cannot be metabolized by human cells. Elimination occurs primarily via the kidneys.

All clinics participating in the study are approved by Competent authorities in Europe and US and are initiating patient screening. OxThera announces completion of recruitment in Phase 3 ePHex study with Oxabact® in patients with primary hyperoxaluria Mon, Apr 06, 2020 07:40 CET OxThera AB, a privately-held biopharmaceutical company dedicated to improving the lives of people with Primary Hyperoxaluria (PH), announced today that it has completed enrollment in its Oxabact ePHex phase III study. OxThera initiates extension part of a Phase 3 study of Oxabact in Primary Hyperoxaluria Thu, Jun 20, 2019 10:00 CET OxThera AB, a biopharmaceutical company dedicated to improve the lives of people living with Primary Hyperoxaluria, today announced that the first patients in a Phase 3 study of Oxabact® have completed the study and transitioned to an open-label extension part. OxThera initiates extension part of a Phase 3 study of Oxabact in Primary Hyperoxaluria (Cision) 2019-06-20 10:00 OxThera AB, a biopharmaceutical company dedicated to improve the lives of people living with Primary Hyperoxaluria, today announced that the first patients in a Phase 3 study of Oxabact® have completed the study and transitioned to an open-label extension part.

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OxThera is a biopharmaceutical company with products in late stage clinical development focusing on Primary and Secondary Hyperoxaluria. OxThera currently

All clinics participating in the study are approved by Competent authorities in Europe and US and are initiating patient screening. ‘We are pleased to announce that we are now fully open for enrolment STOCKHOLM, SWEDEN – June 20, 2019. OxThera AB, a biopharmaceutical company dedicated to improve the lives of people living with Primary Hyperoxaluria, today announced that the first patients in a Phase 3 study of Oxabact® have completed the study and transitioned to an open-label extension part. ePHex - An OxThera Clinical Trial in Primary Hyperoxaluria, Stockholm, Sweden. 39 likes.

2018-07-10

Primary Hyperoxaluria (PH) is a rare autosomal recessive inborn error of to OxThera AB, Sweden, for Oxalobacter formigenes strain HC-1 for the treatment of primary hyperoxaluria. The sponsor's address was updated in June 2018. Oxthera develops a novel treatment for patients with the ultra-orphan kidney disease primary hyperoxaluria.

/PRNewswire/ -- OxThera AB has been granted three Japanese patents during 2012 and 2013. The patents will secure the pharmaceutical composition and the method OxThera AB, a privately-held biopharmaceutical company dedicated to improving the lives of people with Primary Hyperoxaluri OxThera receives positive decision from EMA on Paediatric Investigational Plan (PIP) for treatment of primary hyperoxaluria with Oxalobacter formigenes | Placera OxThera AB, a Stockholm-based privately-held biopharmaceutical company, announced that the Phase 3 study with Oxabact ® in Primary Hyperoxaluria (PH) is now fully open for recruitment. All clinics participating in the study are approved by Competent authorities in Europe and US and are initiating patient screening. STOCKHOLM, June 20, 2019 /PRNewswire/ -- OxThera AB, a biopharmaceutical company dedicated to improve the lives of people living with Primary Hyperoxaluria, today announced that the first patients in a Phase 3 study of Oxabact ® have completed the study and transitioned to an open-label extension part. OxThera is a biopharmaceutical company with products in late stage clinical development focusing on Primary and Secondary Hyperoxaluria.