Evidence map›Paper›PMID 35170192›Full record

ArticleDiabetes, obesity & metabolism2022

Effect of bremelanotide on body weight of obese women: Data from two phase 1 randomized controlled trials.

Carl Spana, Robert Jordan, Steven Fischkoff

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, obesity & metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 13 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

3 authors at 2 institutions in 1 country.

Carl SpanaPalatin Technologies, Inc., Cranbury, New Jersey, USA.ORCID 0000-0001-9705-6155
Robert JordanPalatin Technologies, Inc., Cranbury, New Jersey, USA.
Steven FischkoffFlame Biosciences, New Hope, Pennsylvania, USA.
Palatin Technologies (United States) · USProject HOPE · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe melanocortin 4 receptor (MC4R) plays a central role in appetite regulation, and agonistic activity at this receptor promotes satiety. Results from two randomized controlled clinical trials examine the effects of bremelanotide's agonism at MC4R on caloric intake and body weight.

methodsPremenopausal women with a body mass index >30 kg/m

resultsIn Study A, 27 of 30 bremelanotide subjects (90.0%) completed the trial and exhibited a significantly greater reduction in body weight after 16 days versus placebo [least squares mean difference (95% CI), -1.3 (-1.9 to -0.8) kg; p < .0001]. Mean caloric intake in bremelanotide subjects was decreased versus placebo, with a magnitude of reduction of approximately 400 kcal/day throughout Study A (p < .01). In Study B, 15 of 27 subjects (55.6%) completed all three phases. Significantly greater reduction of mean body weight occurred in twice-daily bremelanotide subjects versus placebo (1.7 vs. 0.9 kg, respectively, p < .001). Total caloric intake reduction was significantly greater in the bremelanotide groups versus placebo (mean difference range: 398-469 kcal; p < .0001).

conclusionsAgonist activity at the MC4R may aid in reducing caloric intake and weight loss in obese women.

Indexed as

alpha-MSHObesityPeptides, CyclicBody WeightClinical Trials, Phase I as TopicDouble-Blind MethodFemaleHumansRandomized Controlled Trials as Topicalpha-MSHbremelanotidePeptides, CyclicbremelanotideMC4r agonistmelanocortinobesityweight loss

Identifiers

PMID35170192
PMCPMC9314948
OpenAlexW4212850195

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.