Corbus begins phase 1 trial for advanced solid tumors

Published 09/12/2024, 13:14
Corbus begins phase 1 trial for advanced solid tumors
CRBP
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NORWOOD – Corbus Pharmaceuticals (NASDAQ:CRBP) Holdings, Inc. (NASDAQ: CRBP), a $186 million market cap company specializing in oncology and obesity treatments, has initiated the Phase 1 clinical trial of its drug candidate CRB-601, designed for patients with advanced solid tumors. According to InvestingPro data, the stock has shown remarkable resilience with a 186% return over the past year, despite recent volatility. This marks the first time a patient has been dosed in the study, which is aimed at evaluating the safety and preliminary efficacy of the monoclonal antibody.

CRB-601 targets the activation of latent TGFβ by blocking integrin αVβ8, a mechanism that is believed to play a role in tumor immune evasion. Preclinical studies have shown that CRB-601 may enhance the effectiveness of immune checkpoint inhibitors, which are a class of drugs used in cancer immunotherapy.

The Chief Medical (TASE:PMCN) Officer of Corbus, Dr. Dominic Smethurst, expressed optimism about the potential of CRB-601 to modulate TGFβ signaling and its implications for mobilizing the immune system against tumors. Dr. Jeffrey M. Clarke, a principal investigator in the study, also highlighted the significance of this clinical trial in advancing the understanding of immunotherapy treatments. The company maintains a strong financial position with a healthy current ratio of 13.8 and minimal debt-to-equity ratio of 0.02, as reported by InvestingPro.

Corbus's diversified portfolio also includes CRB-701, a next-generation antibody drug conjugate targeting Nectin-4 on cancer cells, and CRB-913, a treatment for obesity. The company's approach focuses on leveraging scientific advancements to address biological pathways related to serious illnesses.

The press release also contained forward-looking statements regarding the company's expectations for trial results, development timelines, and market opportunities. While these statements reflect the company's beliefs based on current information, they involve risks and uncertainties that could cause actual results to differ materially.

Investors are advised that the information in this article is based on a press release statement from Corbus Pharmaceuticals and should not place undue reliance on forward-looking statements which are subject to change. Analysts maintain a strong buy consensus with price targets ranging from $35 to $75. For deeper insights into Corbus's financial health, valuation metrics, and additional ProTips, investors can access the comprehensive Pro Research Report available on InvestingPro.

In other recent news, Corbus Pharmaceuticals has made significant strides in its clinical trials, with the U.S. Food and Drug Administration fast-tracking its investigational drug, CRB-701, for the treatment of metastatic cervical cancer. The company has completed enrollment for its Phase 1 clinical trial for CRB-701 and anticipates reporting initial data in the first quarter of 2025. Furthermore, Corbus Pharmaceuticals reported strong third-quarter results, with an ending cash total of $159 million, projected to fund operations until the second half of 2027.

In terms of analyst attention, Piper Sandler initiated coverage on Corbus with an Overweight rating and a price target of $35.00, while Oppenheimer maintained its Outperform rating and $60.00 price target. B.Riley reduced its price target to $40 from $85, maintaining a Buy rating, and Mizuho (NYSE:MFG) Securities also maintained its Outperform rating, with a price target set at $74.00.

In addition, Corbus Pharmaceuticals is also developing CRB-913, a potential treatment for obesity, with Phase 1 trials slated to begin in the first quarter of 2025. Lastly, Anne Altmeyer Ph.D., a board member, initiated a prearranged trading plan for her shares in the company. These developments highlight the ongoing progress and positive analyst outlook for Corbus Pharmaceuticals.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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