Evidence map›Paper›PMID 19638959›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2009

Phase I study of H5.020CMV.PDGF-beta to treat venous leg ulcer disease.

David J Margolis, Lee M Morris, Maryte Papadopoulos, Linda Weinberg, Jennifer C Filip, Stephanie A Lang, Sachin S Vaikunth, Timothy M Crombleholme

Open access · hybridAbstract readClinical Trial, Phase I
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Preclinical model for phenotypic correction of dystrophic epidermolysis bullosa byMolecular therapy. Methods & clinical development · 2022
    Article
  4. Review
  5. Review
  6. Adenovirus-Antibody Complexes Contributed to Lethal Systemic Inflammation in a Gene Therapy Trial.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Gene therapy for skin diseases.Cold Spring Harbor perspectives in medicine · 2014
    Review
  15. Venous leg ulcerations: a treatment update.Current treatment options in cardiovascular medicine · 2010
    Article
  16. Review
  17. Clinical application of growth factors and cytokines in wound healing.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    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

8 authors at 2 institutions in 1 country.

David J MargolisCenter for Clinical Epidemiology and Biostatistics, 815 Blockley Hall, 423 Guardian Drive, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA. margo@mail.med.upenn.edu
Lee M Morris
Maryte Papadopoulos
Linda Weinberg
Jennifer C Filip
Stephanie A Lang
Sachin S Vaikunth
Timothy M Crombleholme
University of Pennsylvania · USCincinnati Children's Hospital Medical Center · US

Funding

INSTITUTIONAL CLINICAL AND TRANSLATIONAL SCIENCE AWARDUL1RR024134 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2006 to 2011
$70.4M
PATIENT ORIENTED RESEARCH IN CHRONIC WOUNDSK24AR002212 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI MARGOLIS, DAVID · 2001 to 2010
$1.3M
PILOT TRIAL ON INNOVATIVE THERAPY FOR VENOUS LEG ULCER-264992238N01AR092238 · NIAMS · UNIVERSITY OF PENNSYLVANIA · 1999 to 2003
–
NCRR NIH HHS UL1 RR024134NCRR NIH HHS UL1RR024134NIAMS NIH HHS K24 AR002212NIAMS NIH HHS K24AR002212NIAMS NIH HHS N01 AR092238
6 · The paper itself

Abstract

Venous leg ulcers are a prevalent nonhealing wound of the lower extremity. Although topically applied growth factors successfully improve wound repair in animal studies, similar studies on humans with venous leg ulcers have not been successful. This study was designed to evaluate the acute safety and biologic feasibility of peri-ulcer injection of a replication-incompetent adenoviral construct expressing platelet-derived growth factor-beta (PDGF-beta). In this phase I study, we demonstrate the initial safety, feasibility, and biologic plausibility of using H5.020CMV.PDGF-beta to treat venous leg ulcer disease.

Indexed as

AdenoviridaeAdultCytomegalovirusEnhancer Elements, GeneticFemaleGenetic TherapyGenetic VectorsHumansLeg UlcerMaleMiddle AgedNeovascularization, PhysiologicPlatelet-Derived Growth FactorPromoter Regions, GeneticTreatment OutcomeVaricose UlcerPlatelet-Derived Growth Factor

Identifiers

PMID19638959
PMCPMC2835007
OpenAlexW2023307607

What OpenQuestion holds

Textmetadata
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.