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The Company is currently developing and commercializing roxadustat, an oral small molecule inhibitor of HIF prolyl hydroxylase activity, for anemia associated with chronic kidney disease CKD. Roxadustat corrected and maintained hemoglobin in non-dialysis dependent patients with anemia using similar doses regardless of iron status at baseline. Pacific Time to discuss financial results and provide a business update. Investors: Michael Tung, M. Investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this release, and we undertake no obligation to update any forward-looking statement in this press release, except as required by law. To access the replay, please dial domestic or international and use passcode About Roxadustat Roxadustat is a first-in-class, orally administered small molecule HIF-PH inhibitor that promotes erythropoiesis through increasing endogenous production of erythropoietin, and improved iron absorption, transport and mobilization. NDA review and E. Roxadustat reduced the risk of red blood cell transfusion during anemia treatment in dialysis dependent CKD patients vs. Astellas and FibroGen are collaborating on the development and commercialization of roxadustat for the treatment of anemia in territories including Japan and Europe. Roxadustat U. Media Inquiries: Sara Iacovino 1.

Skip to main content. Japan sNDA for roxadustat for the treatment of anemia of chronic kidney lapc 2020 results CKD in non-dialysis-dependent patients is under https://agency-people.ru/2020/new-south-dakota-laws-2020.html. Upcoming Events.

Our partner Astellas expects the Marketing Authorization Application filing for roxadustat for the treatment of anemia in CKD in the second quarter of Roxadustat is also in clinical development for anemia associated with myelodysplastic syndromes MDS and for chemotherapy-induced anemia.

Contact: FibroGen, Inc. Our actual results may differ materially from those indicated in these forward-looking statements due to risks and uncertainties related to the continued progress and timing of our various programs, including the enrollment and results from ongoing and potential future clinical trials, and other matters that are described in our Annual Report on Form K for the fiscal year ended December 31, and our Quarterly Report on Form Q for quarter ended March 31, filed with the Securities and Exchange Commission SECincluding the risk factors set forth therein.

Pamrevlumab, an anti-CTGF human monoclonal antibody, is in clinical development for the treatment of idiopathic pulmonary fibrosis IPFlocally advanced unresectable pancreatic cancer, and Duchenne muscular dystrophy DMD.

In Europe, the Marketing Authorization Lapc 2020 results filing for roxadustat for the treatment of anemia in both dialysis- and non-dialysis-dependent patients with CKD is lapc 2020 results in the second quarter of Corporate and Financial.

Roxadustat is approved in China for the treatment of anemia in CKD patients on dialysis and patients not on dialysis, and is approved in Japan for the treatment of anemia in CKD patients on dialysis, and a supplemental NDA for the treatment of anemia in CKD patients not on dialysis is under regulatory review. Presented new analyses from our Phase 3 roxadustat trials at the annual National Kidney Foundation Spring Clinical meeting which demonstrated:. A replay of the webcast will be available shortly after the call for a period of two weeks. Roxadustat reduced the risk of red blood cell transfusions and IV iron rescue compared to placebo in non-dialysis CKD patients, regardless of iron status at baseline. For information about pamrevlumab studies currently recruiting patients, please visit www. Eastern Time p. For more information, please visit www. AstraZeneca and FibroGen are collaborating on the development and commercialization of roxadustat for the treatment of anemia in the U. To participate in the conference call by telephone, please dial 1 U. Our strong financial position gives us sufficient runway to navigate this storm. With pamrevlumab, our monoclonal antibody targeting connective tissue growth factor CTGF , we are implementing a comprehensive plan to accelerate development across the three indications of idiopathic pulmonary fibrosis IPF , locally advanced unresectable pancreatic cancer LAPC , and Duchenne muscular dystrophy DMD once the situation with COVID improves. The company applies its pioneering expertise in hypoxia-inducible factor HIF and connective tissue growth factor CTGF biology to advance innovative medicines to treat unmet needs. Pamrevlumab is in Phase 3 clinical development for the treatment of idiopathic pulmonary fibrosis IPF and locally advanced unresectable pancreatic cancer LAPC , and in Phase 2 clinical development for the treatment of Duchenne muscular dystrophy DMD. This trial will enroll approximately 90 patients randomized to placebo and have a treatment period of 52 weeks. Published: May 07, Nevertheless, I want to reassure patients, healthcare providers, and stakeholders of our continued commitment to bring to patients our potential first-in-class medicines for the treatment of chronic and life-threatening conditions. About Pamrevlumab Pamrevlumab is a first-in-class antibody developed by FibroGen that inhibits the activity of connective tissue growth factor CTGF , a common factor in fibrotic and proliferative disorders.