Evidence map›Paper›PMID 12887268›Full record

ReviewDrugs2003

Tipranavir.

Greg L Plosker, David P Figgitt

Abstract readReview
PubMed Publisher
In one paragraph

Review in Drugs, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Therapeutic potential of HIV-1 entry inhibitor peptidomimetics.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Viral protease inhibitors.Handbook of experimental pharmacology · 2009
    Review
  8. Review
  9. Article
  10. New antiretroviral drugs in clinical use.Indian journal of pediatrics · 2006
    Review
  11. Inhibitors of virus replication: recent developments and prospects.Applied microbiology and biotechnology · 2005
    Review
  12. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Greg L PloskerAdis International Limited, Auckland, New Zealand. demail@adis.co.nz
David P Figgitt

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tipranavir is a potent and selective non-peptidic HIV-1 protease inhibitor with a markedly improved resistance profile compared with traditional, peptidomimetic protease inhibitors. The presence of five or fewer protease gene mutations or one or two protease inhibitor resistance-associated mutations (PRAMs) is associated with reduced susceptibility to currently available protease inhibitors. However, 16-20 mutations (including three or more PRAMs) may be needed to confer resistance to tipranavir. Tipranavir-based therapy achieved sustained viral suppression for more than 48 weeks in a small phase II trial in multiple protease inhibitor-experienced HIV-infected patients. A large dose-finding study demonstrated potent virological reduction through 14 days of functional monotherapy in heavily pretreated HIV-infected patients with 6 to >20 protease gene mutations at baseline. Two large, ongoing, phase III trials in patients with multi-drug resistant HIV infection are comparing the efficacy of tipranavir/ritonavir 500/200mg twice daily plus a patient-individualised background antiretroviral regimen versus other ritonavir-boosted protease inhibitor regimens. In general, tipranavir has been well tolerated in clinical trials. As with other protease inhibitors, the most common adverse events with tipranavir have been gastrointestinal disturbances.

Indexed as

Clinical Trials as TopicDose-Response Relationship, DrugDrug Administration ScheduleDrug Resistance, ViralHIV-1HIV InfectionsHIV ProteaseHIV Protease InhibitorsHumansMutationPyridinesPyronesSulfonamidesHIV ProteaseHIV Protease InhibitorsPyridinesPyronesSulfonamidestipranavir

Identifiers

PMID12887268
OpenAlexW3191422891

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.