Evidence map›Paper›PMID 25902795›Full record

ReviewOrphanet journal of rare diseases2015

The TREAT-NMD advisory committee for therapeutics (TACT): an innovative de-risking model to foster orphan drug development.

Emma Heslop, Cristina Csimma, Volker Straub, John McCall, Kanneboyina Nagaraju, Kathryn R Wagner, Didier Caizergues, Rudolf Korinthenberg, Kevin M Flanigan, Petra Kaufmann and 6 more

Open access · goldAbstract readReview
In one paragraph

Review in Orphanet journal of rare diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Mouse models for muscular dystrophies: an overview.Disease models & mechanisms · 2020
    Review
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  9. Article
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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

16 authors at 11 institutions in 4 countries.

Emma HeslopNewcastle University, Newcastle upon Tyne, UK. Emma.Heslop@ncl.ac.uk.
Cristina CsimmaCydan Developments Inc, Cambridge, USA. ccsimma@CydanCo.com.
Volker StraubNewcastle University, Newcastle upon Tyne, UK. volker.straub@newcastle.ac.uk.
John McCallPharMac LLL, Boca Grande, USA. john.m.mccall@pharmacllc.com.
Kanneboyina NagarajuChildren's National Medical Center, Washington, USA. knagaraju@cnmcresearch.org.
Kathryn R WagnerJohns Hopkins University, Baltimore, USA. wagnerk@kennedykrieger.org.
Didier CaizerguesGenethon, Evry, France. caizerg@genethon.fr.
Rudolf KorinthenbergUniversity of Freiburg, Freiburg, Germany. rudolf.korinthenberg@uniklinik-freiburg.de.
Kevin M FlaniganNationwide Children's Hospital, Columbus, USA. kevin.flanigan@nationwidechildrens.org.
Petra KaufmannNational Institutes of Health, Washington, USA. Petra.Kaufman@nih.gov.
Elizabeth McNeilNational Institutes of Health, Washington, USA. mcneilde@ninds.nih.gov.
Jerry MendellNationwide Children's Hospital, Columbus, USA. Jerry.Mendell@nationwidechildrens.org.
Sharon HesterleeParent Project Muscular Dystrophy, New Jersey, USA. sharon.hesterlee@myotonic.org.
Dominic J WellsRoyal Veterinary College, London, UK. dwells@rvc.ac.uk.
Kate BushbyNewcastle University, Newcastle upon Tyne, UK. Kate.Bushby@ncl.ac.uk.
TACT
Newcastle University · GBNational Institutes of Health · USNationwide Children's Hospital · USAmerican Pharmacists Association · USChildren's National · USCytel (United States) · USGenethon (France) · FRJohns Hopkins University · USParent Project Muscular Dystrophy · USRoyal Veterinary College · GBUniversity of Freiburg · DE

Funding

Medical Research Council MR/K000608/1Medical Research Council MR/K501074/1
6 · The paper itself

Abstract

Despite multiple publications on potential therapies for neuromuscular diseases (NMD) in cell and animal models only a handful reach clinical trials. The ability to prioritise drug development according to objective criteria is particularly critical in rare diseases with large unmet needs and a limited numbers of patients who can be enrolled into clinical trials. TREAT-NMD Advisory Committee for Therapeutics (TACT) was established to provide independent and objective guidance on the preclinical and development pathway of potential therapies (whether novel or repurposed) for NMD.We present our experience in the establishment and operation of the TACT. TACT provides a unique resource of recognized experts from multiple disciplines. The goal of each TACT review is to help the sponsor to position the candidate compound along a realistic and well-informed plan to clinical trials, and eventual registration. The reviews and subsequent recommendations are focused on generating meaningful and rigorous data that can enable clear go/no-go decisions and facilitate longer term funding or partnering opportunities. The review process thereby acts to comment on viability, de-risking the process of proceeding on a development programme.To date TACT has held 10 review meeting and reviewed 29 program applications in several rare neuromuscular diseases: Of the 29 programs reviewed, 19 were from industry and 10 were from academia; 15 were for novel compounds and 14 were for repurposed drugs; 16 were small molecules and 13 were biologics; 14 were preclinical stage applications and 15 were clinical stage applications. 3 had received Orphan drug designation from European Medicines Agency and 3 from Food and Drug Administration. A number of recurrent themes emerged over the course of the reviews and we found that applicants frequently require advice and education on issues concerned with preclinical standard operating procedures, interactions with regulatory agencies, formulation, repurposing, clinical trial design, manufacturing and ethics.Over the 5 years since its establishment TACT has amassed a body of experience that can be extrapolated to other groups of rare diseases to improve the community's chances of successfully bringing new rare disease drugs to registration and ultimately to market.

Indexed as

Orphan Drug ProductionAdvisory CommitteesAnimalsHumansNeuromuscular DiseasesRare DiseasesUnited States

Identifiers

PMID25902795
PMCPMC4417237
OpenAlexW2134573391

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.