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Updated: Jun 9, 2025

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
Published on: December 11, 2016
Pathways for non-manufacturers to drive generic drug repurposing for cancer in the U.S
Devon Crittenden1, Raquel Gallagher1, Fernanda Milans Del Bosch1
1Reboot Rx Inc, Boston, MA, United States.
Abstract:
Repurposing generic drugs as new treatments for life-threatening diseases such as cancer is an exciting yet largely overlooked opportunity due to a lack of market-driven incentives. Nonprofit organizations and other non-manufacturers have been ramping up efforts to repurpose widely available generic drugs and rapidly expand affordable treatment options for patients. However, these non-manufacturers find it difficult to obtain regulatory approval in the U.S. Without a straightforward path for approval and updating drug labeling, non-manufacturers have relied on off-label use of repurposed drugs. This limits the broad clinical adoption of these drugs and patient access. In this paper, we explore the regulatory landscape for repurposing of small molecule generic drugs within the U.S. We describe case studies of repurposed drugs that have been successfully incorporated into clinical treatment guidelines for cancer without regulatory approval. To encourage greater adoption of generic drugs in clinical practice-that is, to encourage the repurposing of these drugs-we examine existing Food and Drug Administration (FDA) pathways for approval of new uses or indications for generic drugs. We show how non-manufacturers, who are generally more active in generic drug repurposing than manufacturers, could utilize existing regulatory authorities and pathways, and we describe the challenges they face. We propose an extension of the existing 505(b)(2) new drug application (NDA) approval pathway, called a "labeling-only" 505(b)(2) NDA, that would enable non-manufacturers to seek approval of new indications for well-established small molecule drugs when multiple generic products are already available. It would not require new chemistry, manufacturing, and controls (CMC) data or introducing new drug products into the marketplace. This pathway would unlock innovation broadly and enable patients to benefit from the enormous potential of low-cost generic drugs.
Insights
Repurposing generic drugs offers affordable treatments for diseases like cancer. A new "labeling-only" pathway could streamline regulatory approval for non-manufacturers, expanding patient access to these vital therapies.
Area of Science:
- Drug repurposing
- Regulatory science
- Oncology therapeutics
Background:
- Generic drug repurposing presents a significant opportunity for affordable disease treatment.
- Non-manufacturers face regulatory hurdles in the U.S. for approving repurposed generic drugs.
- Current reliance on off-label use limits clinical adoption and patient access.
Purpose of the Study:
- To explore the U.S. regulatory landscape for repurposing small molecule generic drugs.
- To examine existing Food and Drug Administration (FDA) pathways for new generic drug indications.
- To propose a novel regulatory pathway to facilitate generic drug repurposing.
Main Methods:
- Analysis of the U.S. regulatory framework for drug approval.
- Review of case studies of successfully repurposed generic drugs in cancer treatment.
- Examination of FDA's 505(b)(2) new drug application (NDA) pathway.
Main Results:
- Non-manufacturers are key drivers of generic drug repurposing but face approval challenges.
- Existing pathways are not optimized for non-manufacturer-led repurposing efforts.
- Successful repurposing has occurred without formal regulatory approval, highlighting unmet needs.
Conclusions:
- A "labeling-only" 505(b)(2) NDA pathway is proposed to streamline approval for new indications of generic drugs.
- This pathway would enable non-manufacturers to gain regulatory approval without new CMC data or products.
- The proposed pathway could unlock innovation and improve patient access to low-cost, effective generic drug treatments.
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