Evidence map›Paper›PMID 40696162›Full record

ArticleCommunications medicine2025

Safety and pharmacokinetics of the non-hormonal male contraceptive YCT-529.

Nadja Mannowetz, Stewart W McCallum, Sharan Sidhu, Karen H Mena, Eric P Ruby, Ramiro Castro-Santamaria, Emily Dodds, Dennis Henderson, Gareth Whitaker, Heather Wright and 3 more

Erratum issued Registry-linked trialAbstract read
In one paragraph

Article in Communications medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT06094283 (Double-blind, Placebo Controlled, First in Human Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Ascending Oral Doses of YCT-529), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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.

NCT06094283 phase1completednot on this map

Double-blind, Placebo Controlled, First in Human Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Ascending Oral Doses of YCT-529

TypeinterventionalSponsorYourChoice Therapeutics, Inc.Ran2023 to 2024Enrolled16ConditionsMale ContraceptionArmsYCT-529, YCT-529 Placebo
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
  2. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Nadja MannowetzYourChoice Therapeutics, San Francisco, USA. nadja@yourchoicetx.com.ORCID http://orcid.org/0009-0005-5198-5473
Stewart W McCallumYourChoice Therapeutics, San Francisco, USA.
Sharan SidhuQuotient Sciences, Nottingham, UK.
Karen H MenaYourChoice Therapeutics, San Francisco, USA.
Eric P RubyYourChoice Therapeutics, San Francisco, USA.
Ramiro Castro-SantamariaIncyte, Wilmington, USA.
Emily DoddsQuotient Sciences, Nottingham, UK.
Dennis HendersonQuotient Sciences, Nottingham, UK.
Gareth WhitakerQuotient Sciences, Nottingham, UK.
Heather WrightQuotient Sciences, Nottingham, UK.
Sarah BeaudoinQuotient Sciences, Nottingham, UK.
Gunda I GeorgCollege of Pharmacy, University of Minnesota, Minneapolis, MN, USA.
Akash BakshiYourChoice Therapeutics, San Francisco, USA. akash@yourchoicetx.com.ORCID http://orcid.org/0009-0007-9892-5421

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSince nearly half of all pregnancies in the US and worldwide are unintended, there is a critical need for additional contraceptive options for men and women. After a hiatus in non-hormonal male contraceptive development of about half a century, the new chemical entity YCT-529 - a retinoic acid receptor-α antagonist - is being developed as a non-hormonal oral male contraceptive to decrease sperm count by impairing retinoic acid signaling in the testes.

methodsHere, we report the results of the first in human Phase 1a clinical trial with YCT-529 to assess its safety, tolerability, pharmacokinetics and pharmacodynamics, and its potential effects on heart rate, inflammatory biomarkers, sexual desire and mood. Sixteen male volunteers were enrolled to receive single oral doses of 10, 30, 90 or 180 mg of YCT-529 in the fasted state. Volunteers also received 30 mg in the fed state to study the effect of food on the pharmacokinetics of YCT-529.

resultsSingle doses of up to 180 mg of YCT-529 had no effects on heart rate, hormone (follicle-stimulating hormone, luteinizing hormone, and testosterone), sex hormone-binding globulin or inflammatory biomarker levels, sexual desire or mood. Further, there was no clear food effect on the pharmacokinetics of YCT-529.

conclusionsOverall, YCT-529 was well tolerated in this single ascending dose study (ClinicalTrials.gov registration: NCT06094283), which is a substantial requirement in contraceptive development.

Identifiers

PMID40696162
PMCPMC12284176

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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.