Evidence map›Paper›PMID 41088407›Full record

ArticleOrphanet journal of rare diseases2025

Perspectives on the FDA platform technology designation program for the approval of gene therapies: a Swiss multi-stakeholder exploratory interview study.

Yi Han, Kelly E Ormond

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Yi HanDepartment of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, ETH Zürich, Zürich, Switzerland.ORCID 0009-0008-0499-9532
Kelly E OrmondHealth Ethics & Policy Lab, Department of Health Sciences and Technology, ETH Zürich, Hottingerstrasse 10, 8092, Zürich, Switzerland. kelly.ormond@hest.ethz.ch.ORCID 0000-0002-1033-0818

Funding

The CRISPR Vision Program: Nonviral Genome Editing Platforms to Treat Inherited Retinal Channelopathies Epqt SupplementU19NS132296 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI Cathy Rasmussen · 2023 to 2026
$36.8M
PaSAGE: PAtient Supported Approaches to Gene EditingR01HG011461 · NHGRI · MAYO CLINIC JACKSONVILLE · PI ALLYSE, MEGAN A., ISASI, ROSARIO · 2022 to 2024
$2.4M
NHGRI NIH HHS R01 HG011461NINDS NIH HHS U19 NS132296
6 · The paper itself

Abstract

backgroundThe U.S. Food and Drug Administration (FDA)'s platform technology designation program aims to streamline the development and approval process for advanced therapy medicinal products and is anticipated to be particularly beneficial for the development of gene therapies for rare and ultra-rare diseases. This is an exploratory interview study of Swiss-based perspectives, including insights from stakeholders in industry, academia, regulation, and reimbursement. The objective of our study is to document Swiss professionals' views on the US platform designation program and to assess the acceptability and feasibility of a similar program in Europe.

resultsParticipants identified benefits such as reduced redundancy in pre-clinical testing, standardization of manufacturing, and increased predictability of regulatory requirements. Concerns were raised about clinical assessment, commercialization strategies, and global regulatory alignment. Though participants anticipate it to increase innovation in the rare disease area, some raised the possibility that technologies may stagnate around a platform, or that designations may quickly become obsolete due to the speed of technological development.

conclusionsThe introduction of the platform technology designation program in the US is a step towards increasing treatment options for ultra-rare diseases. While there is potential for platform designation to enable development in this area, its success will depend on addressing the outlined challenges.

Indexed as

Genetic TherapyHumansRare DiseasesSwitzerlandUnited StatesUnited States Food and Drug AdministrationAdvanced therapy medicinal products (ATMP)Drug developmentGene therapyPharmaceutical regulationPlatform technologyRare disease therapy

Identifiers

PMID41088407
PMCPMC12522643

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.