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Clinical safety of becaplermin (rhPDGF-BB) gel. Becaplermin Studies Group.

Abstract
This overview of the safety of becaplermin gel is based on six well-controlled clinical studies that included patients with lower extremity diabetic neuropathic ulcers. Patients receiving becaplermin gel (n = 538), placebo gel (n = 278), or good ulcer care alone (n = 190) had a similar incidence of ulcer-related adverse events, such as infection, cellulitis, or osteomyelitis. Erythematous rash occurred in 2% of patients with suspected wound infections treated with becaplermin gel and 1% of patients treated with placebo gel. No rashes were observed in patients treated with good ulcer care alone. The incidence of cardiovascular, respiratory, musculoskeletal, and central and peripheral nervous system disorders were similar across all treatment groups. Mortality rates were also similar across all treatment groups. Patients treated with becaplermin gel did not develop neutralizing antibodies against becaplermin. Therefore, becaplermin gel appears to be a safe therapy for the treatment of lower extremity diabetic ulcers.
AuthorsJ M Smiell
JournalAmerican journal of surgery (Am J Surg) Vol. 176 Issue 2A Suppl Pg. 68S-73S (Aug 1998) ISSN: 0002-9610 [Print] United States
PMID9777975 (Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anticoagulants
  • Gels
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Proteins c-sis
  • Recombinant Proteins
  • Becaplermin
Topics
  • Absorption
  • Adult
  • Aged
  • Anticoagulants (adverse effects, pharmacokinetics, therapeutic use)
  • Becaplermin
  • Diabetic Foot (drug therapy)
  • Double-Blind Method
  • Female
  • Gels
  • Humans
  • Male
  • Middle Aged
  • Platelet-Derived Growth Factor (adverse effects, pharmacokinetics, therapeutic use)
  • Proto-Oncogene Proteins c-sis
  • Recombinant Proteins (adverse effects, pharmacokinetics, therapeutic use)
  • Skin Diseases (chemically induced)

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