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NCT05930925
A Study to Understand How the Study Medicine Called ARV-471 is Processed in Healthy Adults
Phase 1 trial testing [phenyl-14C]ARV-471 in Healthy in 12 participants. Completed in 14 August 2023.
27 July 2023
Quick facts
| Lead sponsor | Pfizer |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | other |
| Enrollment | 12 |
| Start date | 12 June 2023 |
| Primary completion | 27 July 2023 |
| Estimated completion | 14 August 2023 |
| Sites | 1 location across United States |
Drugs / interventions tested
- [phenyl-14C]ARV-471 — full drug profile →
- [oxoisoindolin-14C]ARV-471 — full drug profile →
Conditions studied
- Healthy — all drugs for Healthy →
Sponsor
Pfizer — full company profile →
Who can join
18 and older, any sex, with Healthy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of the study is to understand how the study medicine ARV-471 is processed in the body of healthy males and females who do not have the potential to have children. This study is seeking for participants who: * are healthy males and females who do not have the potential to have children. * are 18 years of age or older. * weigh more than 110 pounds.
Publications & conference data
5 peer-reviewed publications reference this trial (live from Europe PMC):
-
PROTAC Technology as a New Tool for Modern Pharmacotherapy.
Kubryń N, Fijałkowski Ł, Nowaczyk J, Jamil A, et al · · 2025 · cited 13× · PMID 40430296 · DOI 10.3390/molecules30102123 -
Proteolysis-Targeting Chimera (PROTAC): Current Applications and Future Directions.
Fan G, Chen S, Zhang Q, Yu N, et al · · 2025 · cited 6× · PMID 41049269 · DOI 10.1002/mco2.70401 -
PROTAC-based protein degradation: a window of opportunity for melanoma therapy.
Gentile G, D'Aguanno S, Di Martile M, Petricca A, et al · · 2026 · PMID 41761284 · DOI 10.1186/s12929-026-01225-2 -
Recent advances in targeting protein degradation for tumor immunotherapy.
Li S, Jin Y, Wu H, Yuan H, et al · · 2025 · PMID 41345706 · DOI 10.1186/s13045-025-01765-4 -
Characterization of preclinical radio ADME properties of ARV-471 for predicting human PK using PBPK modeling.
He Y, Zhu C, Lei P, Yang C, et al · · 2025 · PMID 40496072 · DOI 10.1016/j.jpha.2024.101175
Verify or expand the search:
- PubMed search for NCT05930925
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05930925 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Pfizer
- Last refreshed: 13 September 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05930925.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing