Posted: 19 December 2024
Starpharma (ASX: SPL, US OTC: SPHRY), an innovative biotechnology company with two decades of experience in advancing dendrimer technology from the lab to the patient, today announces a positive development regarding its DEP® SN38 (DEP® irinotecan) program following a meeting with the US Food and Drug Administration (FDA).
The purpose of the meeting was to confirm the regulatory approval pathways and seek regulatory guidance on the design of a Phase 2/3 clinical program aimed at obtaining registration for DEP® SN38 in patients with platinum-resistant ovarian cancer in the US.
Key Outcomes from the Meeting with the US FDA
The FDA agreed with Starpharma’s proposal that DEP® SN38 could be considered for FDA Fast Track designation, acknowledging that platinum-resistant ovarian cancer is a serious condition with significant unmet medical need.
The FDA also agreed that a “505(b)(2)” regulatory approval pathway is appropriate for DEP® SN38, as the product delivers the active moiety of the FDA-approved drug, irinotecan (Camptosar®). The 505(b)(2) pathway allows Starpharma to utilise existing FDA findings of safety and efficacy for an already approved drug, potentially streamlining the approval process by removing the need for some additional studies.
The FDA indicated that DEP® SN38 may qualify for accelerated approval based on an interim analysis of early surrogate endpoints from the proposed Phase 2/3 clinical trial program. Final outcomes will depend on the results of these studies and the overall data package; however, this accelerated approval could provide early access to DEP® SN38 for patients with platinum-resistant ovarian cancer.
The proposed clinical program for achieving both accelerated and full approval of DEP® SN38 involves comparing the safety and efficacy of DEP® SN38—whether alone or in combination with other anticancer agents—against single-agent chemotherapies, such as paclitaxel, topotecan and pegylated liposomal doxorubicin, either as monotherapy or in combination with other agents.
During the meeting, the FDA offered valuable guidance on the study design, particularly in defining the target patient population, study endpoints, and biostatistical aspects. The agency emphasised the importance of ensuring that DEP® SN38 is applicable to a broad range of patients with platinum-resistant ovarian cancer.
Overall, the feedback and collaborative discussions with the FDA reflect a positive and constructive interaction for Starpharma, clarifying the pathways for clinical development and regulatory approval of DEP® SN38. The FDA’s feedback provides confidence for an Investigational New Drug (IND) application for DEP® SN38, which could be advanced by a commercial partner.
Starpharma was supported in the meeting by a team of external clinical, regulatory and biostatistics advisers. Robert L. Coleman, MD FACOG FACS, one of the world’s leading gynaecologic oncologists and experts in the treatment of, and development of new agents for, ovarian cancer, advised Starpharma on its DEP® SN38 development program and attended the FDA meeting as a representative of Starpharma. Dr Coleman provided real-world expertise on the clinical management of ovarian cancer and the design of registrational clinical trials for this indication.
Following the meeting with the FDA, Dr Coleman commented:
“Starpharma’s meeting with the FDA provided clear guidance on the most efficient path forward for the development and eventual registration of DEP® SN38 as a promising new treatment for patients with platinum-resistant ovarian cancer. This disease represents a significant unmet medical need, and the FDA demonstrated a clear, positive intention to work constructively with the company on the DEP® SN38 program, with the goal of bringing a much-needed new therapy to patients with platinum-resistant ovarian cancer as rapidly as possible.”
Cheryl Maley, Starpharma’s Chief Executive Officer, commented:
“While we focus on maximising the value of our DEP® clinical assets, it is important to ensure we have the best asset package for a potential partner. We have worked hard to create a highly attractive opportunity for prospective partners.
“This feedback from the US FDA marks an important milestone, supporting the IND submission, which a partner can advance through further development, registration, and commercialisation. We are encouraged by the FDA’s guidance, which validates our approach and allows us to proceed confidently with the proposed clinical pathways for DEP® SN38.”
