Bio-Path reports positive trial outcomes for cancer treatments

Published 02/13/2025, 08:05 AM
Bio-Path reports positive trial outcomes for cancer treatments

HOUSTON - Bio-Path Holdings, Inc. (NASDAQ:BPTH), a biotechnology company with a market capitalization of $3.1 million, has announced continued progress in its clinical trials for cancer treatments. According to InvestingPro data, while the company maintains a positive cash position relative to debt, its stock has experienced significant volatility in recent months. The company's Phase 1/1b trial of BP1001-A for solid tumors and Phase 2 study of prexigebersen for Acute Myeloid Leukemia (AML) have both shown promising results.

In the ongoing Phase 1/1b trial, a patient with advanced gynecologic cancer experienced a 15% reduction in her primary tumor after receiving six cycles of treatment with BP1001-A, a higher dose of 90 mg/m2. This patient, who had previously undergone multiple lines of chemotherapy and surgeries, has continued to respond well, completing a tenth treatment cycle as of January 2025.

The Phase 2 triple combination study of prexigebersen, venetoclax, and decitabine in AML patients has also been encouraging. Two elderly patients, one female and one male, have remained in complete remission for over two years, following extended treatment cycles.

Peter H. Nielsen, President and CEO of Bio-Path, expressed optimism about the DNAbilize® platform technology's potential to produce drug candidates targeting specific proteins associated with disease-causing gene products. The positive responses observed in these trials are particularly significant given the fragile condition of the patient populations involved.

The Phase 1/1b trial of BP1001-A is currently enrolling patients for higher dose cohorts, with future studies planned to assess the drug's safety and efficacy in combination with other treatments for recurrent ovarian, endometrial, and late-stage pancreatic cancers.

Bio-Path's DNAbilize® technology is central to its strategy of developing a portfolio of RNAi nanoparticle drugs administered via simple intravenous infusion. With an EBITDA of -$12.35 million in the last twelve months and a current ratio of 0.86, the company faces some financial challenges as it advances its pipeline. InvestingPro subscribers can access 12 additional key insights about Bio-Path's financial health and market position, along with comprehensive analysis in the Pro Research Report. Prexigebersen, the company's lead product candidate, is undergoing a Phase 2 study for blood cancers, while BP1001-A, a modification of prexigebersen, is being tested for solid tumors and obesity-related metabolic diseases.

These updates are based on a press release statement from Bio-Path Holdings, Inc. and reflect the company's ongoing efforts to advance its clinical programs and provide new treatment options for cancer patients. Based on InvestingPro's Fair Value analysis, the stock appears to be currently undervalued, despite experiencing a 92% decline over the past year. The company's next earnings report is scheduled for March 7, 2025, which could provide further insights into its financial trajectory.

In other recent news, Bio-Path Holdings, Inc. has been quite active with several developments. The biotech firm reported a net loss of $2.1 million in Q3 2024, an improvement from the previous year's loss of $3.2 million. The company's cash position was reported at $0.6 million as of September 2024.

Bio-Path is making strides in its clinical trials, including a Phase 2 trial for acute myeloid leukemia (AML) and a Phase 1/1b trial for BP1001-A targeting advanced solid tumors. The company is also exploring BP1001-A's potential for treating obesity and Type 2 diabetes, following promising preclinical results.

However, Bio-Path has also faced challenges, including a notice from Nasdaq about potential delisting due to not meeting the minimum bid price requirement. The company has until June 2025 to regain compliance. Additionally, Bio-Path has discontinued Phase 1 trials for BP1002 due to difficulties enrolling patients.

Despite these hurdles, Bio-Path is pushing forward with its clinical development and operations, with key milestones expected in 2025. These recent developments reveal a company actively navigating the challenges and opportunities of the biotech industry.

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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