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TGTX JPM 2025 Presentation 1.13.25.pdf

上传人: c** 编号:604016 2025-02-03 21页 1.47MB

1、FIERCELY FOCUSEDJanuary 2025J.P.Morgan Healthcare Conference 2Forward Looking Safe Harbor StatementThis presentation contains forward-looking statements that involve a number of risks and uncertainties.For those statements,we claim the protection of the safe harbor for forward-looking statements con

2、tained in the Private Securities Litigation Reform Act of 1995.Such forward looking statements include but are not limited to statements regarding expectations for success of our commercial launch and availability of BRIUMVI(ublituximab-xiiy)for relapsing forms of multiple sclerosis(RMS);anticipated

3、 healthcare professional and patient acceptance and use of BRIUMVI for the FDA-approved indications,statements regarding the results of the ULTIMATE I&II Phase 3 studies as well as the long term safety study and BRIUMVI as a potential treatment for RMS and our statements regarding our potential reve

4、nue targets,operating expenses and cash position.Additional factors that could cause our actual results to differ materially include the following:the Companys ability to establish and maintain a commercial infrastructure for BRIUMVI,and to successfully or in the timeframe projected,launch,market an

5、d sell BRIUMVI;the failure to obtain and maintain requisite regulatory approvals,including the risk that the Company fails to satisfy post-approval regulatory requirements,the potential for variation from the Companys projections and estimates about the potential market for BRIUMVI due to a number o

6、f factors,including,further limitations that regulators may impose on the required labeling for BRIUMVI(such as modifications,resulting from safety signals that arise in the post-marketing setting or in the long-term extension study from the ULTIMATE I and II clinical trials);the Companys ability to

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本文主要介绍了TG Therapeutics公司的抗CD20单克隆抗体BRIUMVI(ublituximab-xiiy)在治疗多发性硬化症(RMS)方面的临床试验结果和市场推广情况。BRIUMVI在美国已获得批准,用于治疗RMS,其疗效和安全性在两项 Phase 3 临床试验中得到了验证。数据显示,BRIUMVI能显著降低 RMS 患者的复发率,且安全性良好。自2023年1月上市以来,BRIUMVI在美国市场的销售表现超出了预期。公司预计,到2025财年,BRIUMVI在美国的净销售额将达到约5.25亿美元,全球总销售额将达到约5.4亿美元。此外,TG Therapeutics还计划开展BRIUMVI的皮下注射版本的研究,并探索其在其他自身免疫疾病中的应用。
"BRIUMVI: How Does It Differ from Other MS Treatments?" "Unlocking the Potential: What's Next for TG Therapeutics?" "Inside the Efficacy & Safety Profile of BRIUMVI in RMS"
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