Evidence map›Paper›PMID 36474952›Full record

ArticleOsteoarthritis and cartilage open2022

Time to first and sustained improvement in WOMAC domains among patients with osteoarthritis receiving tanezumab.

D J Hunter, T J Schnitzer, J Hall, D Semel, I Davignon, J C Cappelleri, A G Bushmakin, L Abraham

3 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Osteoarthritis and cartilage open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 34% 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.

NCT02528188 phase3completednot on this map

A phase 3 randomized, double-blind, active-controlled, multicenter study of the long-term safety and efficacy of subcutaneous administration of tanezumab in subjects with osteoarthritis of the hip or knee

TypeinterventionalSponsorPfizerRan2015 to 2019Enrolled3,021ConditionsChronic Pain, Osteoarthritis, Hip, Osteoarthritis, KneeArmsNSAID, Tanezumab 2.5 mg, Tanezumab 5 mg
NCT02697773 phase3completednot on this map

A phase 3 randomized, double-blind, placebo-controlled, multicenter study of the analgesic efficacy and safety of a dose titration regimen for the subcutaneous administration of tanezumab in subjects with osteoarthritis of the hip or knee

TypeinterventionalSponsorPfizerRan2016 to 2018Enrolled698ConditionsOsteoarthritis, Knee, Osteoarthritis, HipArmsPlacebo, Tanezumab 2.5 mg, Tanezumab 2.5mg/5mg
NCT02709486 phase3completednot on this map

A phase 3 randomized, double-blind, placebo-controlled, multicenter study of the analgesic efficacy and safety of the subcutaneous administration of tanezumab in subjects with osteoarthritis of the hip or knee

TypeinterventionalSponsorPfizerRan2016 to 2018Enrolled849ConditionsOsteoarthritis, Hip, Osteoarthritis, KneeArmsTanezumab, Placebo
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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 5 institutions in 3 countries.

D J HunterUniversity of Sydney, Sydney, Australia.
T J SchnitzerNorthwestern University Feinberg School of Medicine, Chicago, IL, USA.
J HallEli Lilly and Company, Indianapolis, IN, USA.
D SemelPfizer Inc, New York, NY, USA.
I DavignonPfizer Inc, Groton, CT, USA.
J C CappelleriPfizer Inc, Groton, CT, USA.
A G BushmakinPfizer Inc, Groton, CT, USA.
L AbrahamPfizer Ltd, Tadworth, UK.
Pfizer (United States) · USEli Lilly (United States) · USNorthwestern University · USPfizer (United Kingdom) · GBThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To assess onset of effect in three placebo- or nonsteroidal anti-inflammatory drug (NSAID)-controlled trials of tanezumab in patients with moderate-to-severe osteoarthritis. Methods: Post-hoc nonparametric Kaplan-Meier analyses were used to estimate median time to first improvement and to sustained improvement in Western Ontario and McMaster Universities Osteoarthritis Index domain (Pain, Physical Function, Stiffness) scores across a range of improvement thresholds (0-100%, in 5% increments). Time to first improvement was defined as the first week scores met the pre-specified threshold. Time to sustained improvement was defined as the first week scores met the pre-specified threshold and were sustained (on average) for the remainder of the treatment period. Results: Across all domains, tanezumab-treated patients had shorter median times to first improvement (at most thresholds) and reached higher levels of improvement than placebo-treated patients. No substantial differences were observed between tanezumab doses (2.5 and 5 ​mg), or between tanezumab and NSAIDs. Most patients experiencing an event of first improvement went on to experience a sustained event. At low thresholds, sustained improvement occurred simultaneously with, or shortly after, first improvement. At higher thresholds, median time to sustained improvement was longer than median time to first improvement. Conclusions: Following initiation of tanezumab treatment, first improvement of osteoarthritis symptoms of 30% was evident within 2-4 weeks and sustained improvement was evident within 2-8 weeks. Time to improvement of 50% was more variable, with first and sustained events expected within 4-16 and 8-24 weeks, respectively. ClinicalTrialsgov identifiers: NCT02697773; NCT02709486; NCT02528188.

Indexed as

Kaplan–MeierOsteoarthritisTanezumabTime to improvementWOMAC

Identifiers

PMID36474952
PMCPMC9718254
OpenAlexW4283769112

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.