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Enliven Therapeutics' Leukemia Candidate Could Challenge Pfizer, AstraZeneca In Broader Target Market: Analyst

Enliven Therapeutics' Leukemia Candidate Could Challenge Pfizer, AstraZeneca In Broader Target Market: Analyst

安联治疗的白血病候选药物可能在更广泛的目标市场上挑战辉瑞、阿斯利康:分析师
Benzinga ·  09/09 14:05

HC Wainwright initiated coverage on Enliven Therapeutics, Inc. (NASDAQ:ELVN) and noted the company as an emerging biotech company developing next-gen precision-oriented small molecules for solid and liquid tumor indications.

HC Wainwright开始对Enliven Therapeutics, Inc.(纳斯达克股票代码:ELVN)进行报道,并指出该公司是一家新兴的生物技术公司,正在开发用于实体和液体肿瘤适应症的下一代精密小分子。

Enliven's pipeline includes:

Enliven 的管道包括:

  • ELVN-001— a tyrosine kinase inhibitor (TKI) targeting mutant BCR::ABL. HC Wainwright highlights that ELVN-001 could meaningfully improve on existing TKI drugs used in chronic myelogenous leukemia, with applicability across multiple lines of therapy.
  • In April, the company released proof of concept data from the Phase 1 trial of ELVN-001 in patients with chronic myeloid leukemia (CML) who are relapsed, refractory, or intolerant to available TKIs.
  • ELVN-001 achieved a cumulative major molecular response (MMR) rate of 44% (7/16) by 12 weeks and demonstrated responses in patients with prior exposure to asciminib and who were TKI-resistant.
  • ELVN-002 is being evaluated in combination with trastuzumab plus chemotherapy or as monotherapy in HER2-driven malignancies within non-small cell lung, colorectal, and metastatic breast cancer, among others.
  • ELVN-001— 一种靶向突变体 BCR:: ABL 的酪氨酸激酶抑制剂 (TKI)。HC Wainwright强调,ELVN-001 可以对用于慢性粒细胞白血病的现有 TKI 药物进行有意义的改进,适用于多种疗法。
  • 4月,该公司发布了针对复发、难治性或对可用 TKI 不耐受的慢性髓系白血病 (CML) 患者的 ELVN-001 一期试验的概念验证数据。
  • ELVN-001 在 12 周内实现了 44%(7/16)的累积主分子反应 (MMR) 率,并且在之前接触过 asciminib 和 TKI 耐药的患者中表现出反应。
  • ELVN-002 正在评估与曲妥珠单抗联合化疗或作为单一疗法治疗非小细胞肺癌、结直肠癌和转移性乳腺癌等 HER2 驱动的恶性肿瘤。

The analyst initiates with a Buy rating and a price target of $37.

分析师最初的评级为买入,目标股价为37美元。

CML is a chronic disease requiring multiple years of continuous treatment. Patients frequently switch therapies due to liabilities of the existing approved drugs, including poor tolerability due to off-target effects and inability to dose to maximal efficacy.

CML 是一种慢性疾病,需要持续多年的治疗。由于现有批准药物的负债,患者经常更换疗法,包括由于脱靶效应导致耐受性差以及无法给药达到最大疗效。

Six approved drugs—Novartis AG's (NYSE:NVS) Gleevec (imatinib), Scemblix (asciminib), and Tasigna (nilotinib), Bristol-Myers Squibb & Co's (NYSE:BMY) Sprycel (dasatinib), Pfizer Inc (NYSE:PFE) Bosulif (bosutinib), and Takeda Pharmaceutical Co Ltd (NYSE:TAK) Iclusig (ponatinib)—generate over $6 billion in annual sales, with each drug bringing in around $500 million. Some even achieve peak annual sales of up to $2 billion despite competition from generic versions.

六种获批准的药物——诺华股份公司(纽约证券交易所代码:NVS)Gleevec(伊马替尼)、Scemblix(asciminib)和塔西尼亚(尼洛替尼)、百时美施贵宝公司(纽约证券交易所代码:BMY)Sprycel(达沙替尼)、辉瑞公司(纽约证券交易所代码:PFE)Bosulif(bosutnib))和武田制药有限公司(纽约证券交易所代码:TAK)Iclusig(波纳替尼)——年销售额超过60亿美元,每种药物的收入约为5亿美元。尽管有来自仿制药的竞争,有些甚至实现了高达20亿美元的峰值年销售额。

HC Wainwright analyst projects that positioning ELVN-001 as a third-line treatment could surpass $500 million in peak annual sales.

HC Wainwright分析师预计,将 ELVN-001 定位为三线疗法的峰值年销售额可能超过5亿美元。

ELVN-002 has the potential to address unmet needs in HER2-mutant NSCLC, CRC, and mBC, where current treatments have limitations. It could challenge competitors like Pfizer's Tukysa and tap into the growing post-AstraZeneca Plc (NASDAQ:AZN) Enhertu market, with sales possibly reaching hundreds of millions.

ELVN-002 有可能解决 HER2 突变体 NSCLC、CRC 和 mBC 中未得到满足的需求,而目前的治疗方法存在局限性。它可能会挑战辉瑞的Tukysa等竞争对手,进入不断增长的后阿斯利康公司(纳斯达克股票代码:AZN)Enhertu市场,销售额可能达到数亿美元。

While Enliven focuses on precision oncology, its target market is broader than that of past agents like Bristol-Myers' Augtyro (repotrectinib) and Roche Holdings AG's (OTC:RHHBY) Rozlytrek (entrectinib).

尽管Enliven专注于精准肿瘤学,但其目标市场比百时美的Augtyro(repotrectinib)和罗氏控股公司(场外交易代码:RHHBY)Rozlytrek(恩曲替尼)等过去的药物更广泛。

Price Action: ELVN stock is up 7.32% at $23.01 at the last check on Monday.

价格走势:周一最后一次支票时,ELVN股价上涨7.32%,至23.01美元。

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