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Monopar Announces Result of Interim Analysis of Phase 2b/3 VOICE Trial Evaluating Validive for Severe Oral Mucositis

Key Takeaway: Monopar Therapeutics announced that its interim analysis of the Phase 2b/3 VOICE trial for Validive, intended for the prevention of severe oral mucositis, showed it did not meet the efficacy threshold of a 15% absolute difference compared to placebo. Consequently, the company will discontinue the study and halt Validive's active development. However, Monopar stated it has adequate funding to support its other ongoing projects beyond the first quarter of 2024. The findings were communicated by an independent Data Safety Monitoring Board, which confirmed no safety concerns with Validive.

Market Sentiment Analysis

POSITIVE FACTORS

  • Monopar has sufficient funds to support ongoing activities beyond Q1 2024.
  • The trial was conducted under the supervision of an independent DSMB.
  • No safety concerns were reported for Validive during the trial.

CONCERNS & RISKS

  • The trial did not meet the pre-defined efficacy threshold for Validive.
  • Monopar plans to discontinue the study and the active development of Validive.
  • The company's focus is shifting to other drugs due to the disappointing trial results.

Full Press Release Details

mnpr_ex991.htm EXHIBIT 99.1
Monopar Announces Result of Interim Analysis of Phase 2b/3 VOICE Trial Evaluating Validive for Severe Oral Mucositis
WILMETTE, Ill, March 27, 2023 - Monopar Therapeutics Inc. (Nasdaq: MNPR), a clinical-stage biopharmaceutical company focused on developing proprietary therapeutics designed to extend life or improve the quality of life for cancer patients, today announced completion of a pre-specified interim analysis for its Validive Phase 2b/3 VOICE trial for the prevention of severe oral mucositis (SOM) in patients undergoing chemoradiotherapy (CRT) for oropharyngeal cancer (OPC). This is an indication for which there is currently no FDA-approved preventative or treatment.
The interim analysis included the first approximately 50% of the total planned patients to be enrolled. It was conducted by an independent Data Safety Monitoring Board (DSMB), which informed the Company that the trial did not meet the pre-defined threshold for efficacy of a 15% absolute difference in SOM prevention between Validive and placebo. The DSMB also reported that there were no safety concerns attributed to Validive. Based on not meeting the pre-specified efficacy threshold, Monopar announced today that it will be discontinuing the study along with the active development of Validive.
"We are very grateful to the patients and investigators who participated in the VOICE trial. The Phase 2b/3 VOICE trial was intended to further evaluate a novel treatment for SOM following the promising signals observed in a prior randomized, double-blinded Phase 2 study with OPC patients. While we are disappointed with the outcome of this study, we are now focused on re-deploying the financial and human resources previously dedicated to Validive in order to advance our Phase 1b camsirubicin clinical trial and our MNPR-101 radiopharmaceutical program partnered with NorthStar Medical Radioisotopes," said Chandler Robinson, MD, Monopar's Chief Executive Officer.
Monopar also noted today that it has sufficient funds to support its currently planned activities further beyond the first quarter of 2024.
About Monopar Therapeutics Inc.
Monopar Therapeutics is a clinical-stage biopharmaceutical company focused on developing proprietary therapeutics designed to extend life or improve the quality of life for cancer patients. Monopar's pipeline consists of camsirubicin (Phase 1b) for the treatment of advanced soft tissue sarcoma; a late-stage preclinical antibody, MNPR-101, for radiopharmaceutical use in advanced cancers; and an early-stage camsirubicin analog, MNPR-202, for various cancers. For more information, visit: www.monopartx.com.
Forward-Looking Statements
Statements contained in this press release regarding matters that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. The words "may," "will," "could," "would," "should," "expect," "plan," "anticipate," "intend," "believe," "estimate," "predict," "project," "potential," "continue," "target" and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Examples of these forward-looking statements include statements concerning: that Monopar remains focused on re-deploying the financial and human resources previously dedicated to Validive to advance its Phase 1b camsirubicin clinical trial and its MNPR-101 radiopharmaceutical program; and that Monopar also noted it has sufficient funds to support its currently planned activities further beyond the first quarter of 2024. The forward-looking statements involve risks and uncertainties including, but not limited to: not successfully recruiting patients in Monopar's Phase 1b camsirubicin clinical trial within expected timeframes, if at all; the Phase 1b camsirubicin clinical trial does not provide safety or efficacy data; MNPR-101 radiopharmaceutical program partnered with NorthStar does not prove safe or efficacious; Monopar does not have sufficient resources to support its currently planned activities further beyond the first quarter of 2024 and is unable to raise funds; and the significant general risks and uncertainties surrounding the research, development, regulatory approval, and commercialization of therapeutics. Actual results may differ materially from those expressed or implied by such forward-looking statements. Risks are described more fully in Monopar's filings with the Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made. Monopar undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made. Any forward-looking statements contained in this press release represent Monopar's views only as of the date hereof and should not be relied upon as representing its views as of any subsequent date.
Monopar Therapeutics Inc.
Chief Financial Officer
Follow Monopar on social media for updates:
Twitter: @MonoparTx LinkedIn: Monopar Therapeutics

Frequently Asked Questions

What is Validive being tested for in the VOICE trial?

Validive is evaluated for the prevention of severe oral mucositis in cancer patients.

Who conducted the interim analysis of the VOICE trial?

The independent Data Safety Monitoring Board conducted the interim analysis.

What were the results of the VOICE trial interim analysis?

The trial did not meet the efficacy threshold, leading to the study's discontinuation.

Will Monopar continue developing Validive?

No, Monopar announced the discontinuation of Validive's active development.

What is Monopar's focus after Validive?

Monopar will focus on advancing the Phase 1b camsirubicin trial and MNPR-101 program.

Last updated: Mar 27, 2023