Greenwich LifeSciences Provides Update on Upcoming Phase III Clinical Trial, FLAMINGO-01
Greenwich LifeSciences (GLSI) has made substantial progress in its Phase III clinical trial, FLAMINGO-01, aimed at preventing breast cancer recurrences. Key developments include the completion of critical study initiation steps, such as securing a Contract Research Organization and obtaining Central Institutional Review Board approval. A total of 25 clinical sites are currently being established, and manufacturing of the GP2 active ingredient has been finalized. The trial will involve approximately 600 patients and aims to assess the efficacy of GP2 immunotherapy in preventing cancer recurrence.
- Completion of critical steps for Phase III trial initiation.
- 25 clinical sites currently in start-up process.
- CRO contracted for management, data handling, and monitoring.
- Approval secured from Central IRB for the study.
- Manufacturing of the third clinical lot of GP2 completed.
- None.
- The GP2 Phase III clinical trial poster was presented in person at the 2021 annual San Antonio Breast Cancer Symposium (SABCS). The Company was a SABCS sponsor and held a clinical trial planning meeting with investigators at the conference. The poster can be seen here.
- Critical steps toward study initiation have been completed, including manufacturing, contracting with clinical trial partners, and setting up infrastructure.
- At least 25 sites are currently in the study start-up process at a variety of university-based hospitals and cooperative networks.
- Industry leaders for the Phase III clinical trial’s Data Safety Monitoring Board have been recruited and the Steering Committee members are being confirmed.
The Company has made significant progress towards study initiation:
- Contract Research Organization (CRO) has been contracted for study start-up, project management, data management, and clinical data monitoring
- Manufacturing of third clinical lot of GP2 using a commercial line has been completed
- Commercial lots of GP2 active ingredient for filing of BLA have been contracted
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- Drug and biological sample storage sites and other study infrastructure have been put in place
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- Clinical trial sites continue in the study start-up process and the Company continues to solicit additional US and international sites and networks for participation in the study
About FLAMINGO-01 and GLSI-100
The Phase III clinical trial will be called FLAMINGO-01 and the combination of GP2 + GM-CSF will be called GLSI-100. The Phase III trial is comprised of 2 blinded, randomized, placebo-controlled arms for approximately 500 HLA-A*02 patients and 1 open label arm of up to 100 patients for all other HLA types. An interim analysis has been designed to detect a hazard ratio of 0.3 in IDFS, where 28 events will be required. An interim analysis for superiority and futility will be conducted when at least half of those events, 14, have occurred. This sample size provides
About Breast Cancer and HER2/neu Positivity
One in eight
About
About GP2 Immunotherapy Immune Response
As previously reported, GP2 immunotherapy generated GP2-specific immune responses, leading to no metastatic breast cancer recurrence in the HER2/neu 3+ population in the Phase IIb clinical trial, thus supporting GP2’s mechanism of action. Statistically significant peak immunity was reached after 6 months of GP2 treatment, as measured in both the Dimer Binding Assay and the DTH skin test. HER2/neu 3+ population immune response was similar to the HER2/neu 1-2+ population immune response, suggesting the potential to treat the HER2/neu 1-2+ population (including triple negative breast cancer) with GP2 immunotherapy in combination with trastuzumab (Herceptin) based products and other clinically active agents. The broad based immune response suggests the potential for GP2 to treat other HER2/neu 1-3+ expressing cancers. For more information on GP2 immune response and clinical data, please visit the Company’s clinical trial tab at https://greenwichlifesciences.com/clinical-trials/.
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Statements in this press release contain “forward-looking statements” that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “target,” “aim,” “should,” "will,” “would,” or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on Greenwich LifeSciences Inc.’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict, including statements regarding the intended use of net proceeds from any offering; consequently, actual results may differ materially from those expressed or implied by such forward-looking statements. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully in the section titled “Risk Factors” in the final prospectus related to the public offering filed with the
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