MONTREAL, May 01, 2025 (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (TSX: GUD) (“Knight”), a pan-American (ex-USA) specialty pharmaceutical company, will release its first quarter 2025 financial results on Thursday, May 8, 2025 prior to market opening. Following the release, Knight will hold a conference call and audio webcast. Knight cordially invites all interested parties to participate in this call. Date: Thursday, May 8, 2025 Time: 8:30 a.m. ET Telephone: Toll Free: 1-888-699-1199 or International 1-41 ...

MONTREAL, April 29, 2025 (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (TSX: GUD) (“Knight”), a pan-American (ex-US) specialty pharmaceutical company, announced today that Samira Sakhia, President and Chief Executive Officer, is scheduled to present a corporate update at the Bloom Burton & Co. Healthcare Investor Conference on Monday, May 5, 2025, at 2:00 p.m. ET at the Metro Toronto Convention Centre (North Building) in Toronto. A copy of the presentation will be available at www.knighttx.com. About Knight ...

Core Insights - 60 Degrees Pharmaceuticals, Inc. has revealed that the actual burden of babesiosis in the U.S. may be significantly higher than CDC statistics indicate, with nearly 3 million Americans potentially diagnosed with the disease [1][2][9] - The survey conducted by the company suggests that babesiosis is underdiagnosed or underreported, indicating a greater demand for effective treatment than current CDC statistics suggest [2][5] - The company is developing treatment candidates for babesiosis and aims to define the commercial market size for these treatments [5][12] Survey Findings - The survey included 6,000 participants and found that 1.26% of respondents reported a diagnosis of babesiosis, equating to approximately 3 million Americans [6][9] - About 17% of those diagnosed with babesiosis reported experiencing illness for six months or more, suggesting at least 570,000 adults may have chronic disease [6][9] - Approximately 3.7% of respondents reported experiencing chronic fatigue lasting longer than six months, which may be related to babesiosis [7][9] Medical Implications - Babesiosis is a serious tick-borne disease that can co-occur with Lyme disease and may be life-threatening for immunocompromised and elderly individuals [3][10] - There is a hypothesis that persistent Babesia infection may contribute to chronic fatigue, potentially affecting millions of Americans who are undiagnosed [4][8] - The company is conducting clinical trials to test the efficacy of ARAKODA (tafenoquine) in treating babesiosis, although it is currently only approved for malaria prophylaxis [12][13] Company Background - 60 Degrees Pharmaceuticals, Inc. was founded in 2010 and specializes in developing new medicines for infectious diseases [14] - The company achieved FDA approval for its lead product, ARAKODA, in 2018 for malaria prevention and collaborates with research organizations in multiple countries [14]

Core Insights - Knight Therapeutics Inc. has launched Minjuvi® (tafasitamab) in Mexico through its affiliate Grupo Biotoscana de Especialidad S.A. de C.V. [1] - Minjuvi® is indicated for adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) who are not eligible for autologous stem cell transplantation (ASCT) [2][4]. Company Overview - Knight Therapeutics Inc. is a pan-American specialty pharmaceutical company focused on acquiring and commercializing pharmaceutical products in Canada and Latin America [12]. - The company entered a supply and distribution agreement with Incyte for exclusive rights to distribute tafasitamab in Latin America [7]. Product Details - Minjuvi® is a humanized Fc-modified cytolytic CD19 targeting monoclonal antibody, demonstrating a 60% objective response rate (ORR) in clinical trials [4][8]. - The L-MIND trial showed a complete response rate (CR) of 43% and a disease control rate (DCR) of 74% for Minjuvi® in combination with lenalidomide [4]. Clinical Significance - DLBCL is the most common subtype of non-Hodgkin lymphoma, with many patients facing poor prognosis due to refractory disease or relapse [3]. - Approximately 57% of patients responding to Minjuvi® remained in remission at 5 years, highlighting its effectiveness as a treatment option [5]. Regulatory Approval - Minjuvi® received marketing authorization in Mexico based on the L-MIND trial data and was recognized as an orphan medicine by COFEPRIS [4][7]. - The product has also received accelerated approval in the United States and conditional marketing authorization in Europe for similar indications [9].