Evidence map›Paper›PMID 9371346›Full record

Trial reportAntimicrobial agents and chemotherapy1997

Exposure-response relationships for saquinavir, zidovudine, and zalcitabine in combination therapy.

G F Vanhove, J M Gries, D Verotta, L B Sheiner, R Coombs, A C Collier, T F Blaschke

Registry-linked trialOpen access · bronzeAbstract readClinical TrialClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00001040 (Double-Blind, Randomized, Phase II Study of Ro 31-8959 Plus Zidovudine), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 13% 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.

NCT00001040 phase2completednot on this map

Double-Blind, Randomized, Phase II Study of Ro 31-8959 Plus Zidovudine (AZT) Versus AZT Plus Zalcitabine (Dideoxycytidine; ddC) Versus Ro 31-8959 Plus AZT Plus ddC

TypeinterventionalSponsorHoffmann-La RocheEnrolled300ConditionsHIV InfectionsArmsSaquinavir, Zidovudine, Zalcitabine
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 49 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

G F VanhoveDivision of Clinical Pharmacology, Stanford University, California, USA.
J M Gries
D Verotta
L B Sheiner
R Coombs
A C Collier
T F Blaschke
Stanford University · US

Funding

WOMEN'S HEALTH AGENDAU01AI027663 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HAVLIR, DIANE V · 1988 to 2006
$11.4M
WOMEN'S HEALTH AGENDAU01AI027666 · NIAID · STANFORD UNIVERSITY · PI ZOLOPA, ANDREW RICHARD · 1988 to 2006
$11.4M
WOMEN'S HEALTH AGENDAU01AI027664 · NIAID · UNIVERSITY OF WASHINGTON · PI COLLIER, ANN CORNWALL · 1988 to 2006
$11.4M
NIAID NIH HHS AI 27663NIAID NIH HHS AI 27664NIAID NIH HHS AI 27666
6 · The paper itself

Abstract

The relationship of CD4+ cell response, level of RNA in plasma, and quantitative peripheral blood mononuclear cell (PBMC) titer to apparent drug exposure was investigated by using data from AIDS Clinical Trial Group protocol 229, a multicenter randomized study. Patients received either saquinavir, zalcitabine, or a combination of both, along with open-label zidovudine. Approximately 100 patients were enrolled in each arm, and the primary study duration was 24 weeks. Individual drug exposure, the area under the concentration-time curve, was estimated by using population-based pharmacokinetic methods. Response was defined as the maximum increase in CD4+ cell count or the maximum decrease in RNA in plasma or PBMC titer adjusted for baseline CD4+ cell count, RNA in plasma, and PBMC titer, respectively. Regression of responses on exposure demonstrated an exposure effect for saquinavir which was significant for the maximum increase in CD4+ cell count and the decrease in RNA in plasma. For the PBMC titer, no significant relationship could be demonstrated but the results suggested a trend similar to that of the other response variables. For all three response variables, the slope of the saquinavir exposure response was greater with the triple combination (saquinavir, zidovudine, and zalcitabine) than with the combination of saquinavir and zidovudine, suggesting possible synergism between saquinavir and zalcitabine.

Indexed as

AdultAnti-HIV AgentsArea Under CurveCD4 Lymphocyte CountDose-Response Relationship, DrugDrug Therapy, CombinationFemaleHIV InfectionsHumansMaleMiddle AgedRNA, ViralSaquinavirZalcitabineZidovudineAnti-HIV AgentsRNA, ViralSaquinavirZalcitabineZidovudine

Identifiers

PMID9371346
PMCPMC164141
OpenAlexW2133448156

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.