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NCT03834584
A Study of AG-636 in the Treatment of Subjects With Advanced Lymphoma
Phase 1 trial testing AG-636 in Lymphoma in 11 participants. Terminated before completion.
17 June 2020
Quick facts
| Lead sponsor | Agios Pharmaceuticals, Inc. |
|---|---|
| Phase | Phase 1 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 11 |
| Start date | 24 May 2019 |
| Primary completion | 17 June 2020 |
| Estimated completion | 17 June 2020 |
| Sites | 6 locations across United States |
Drugs / interventions tested
- AG-636 — full drug profile →
Conditions studied
- Lymphoma — all drugs for Lymphoma →
Sponsor
Agios Pharmaceuticals, Inc. — full company profile →
Who can join
18 and older, any sex, with Lymphoma. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study will evaluate the safety, pharmacokinetics, pharmacodynamics, and clinical activity of AG-636, an oral Dihydroorotate Dehydrogenase (DHODH) inhibitor, in subjects with advanced lymphoma.
Publications & conference data
8 peer-reviewed publications reference this trial (live from Europe PMC):
-
Dysregulated haematopoietic stem cell behaviour in myeloid leukaemogenesis.
Yamashita M, Dellorusso PV, Olson OC, Passegué E. · · 2020 · cited 128× · PMID 32415283 · DOI 10.1038/s41568-020-0260-3 -
Small-molecule agents for cancer immunotherapy.
Wang F, Fu K, Wang Y, Pan C, et al · · 2024 · cited 41× · PMID 38486980 · DOI 10.1016/j.apsb.2023.12.010 -
Targeting Acute Myelogenous Leukemia Using Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on the 2-Hydroxypyrazolo[1,5-<i>a</i>]pyridine Scaffold: SAR of the Biphenyl Moiety.
Sainas S, Giorgis M, Circosta P, Gaidano V, et al · · 2021 · cited 26× · PMID 33844533 · DOI 10.1021/acs.jmedchem.0c01549 -
DHODH-mediated mitochondrial redox homeostasis: a novel ferroptosis regulator and promising therapeutic target.
Cao J, Chen X, Chen L, Lu Y, et al · · 2025 · cited 23× · PMID 40716151 · DOI 10.1016/j.redox.2025.103788 -
Small molecule inhibitors for cancer metabolism: promising prospects to be explored.
Liu D, Wang H, Li X, Liu J, et al · · 2023 · cited 6× · PMID 37002510 · DOI 10.1007/s00432-022-04501-4 -
DHODH Inhibition Suppresses <i>MYC</i> and Inhibits the Growth of Medulloblastoma in a Novel In Vivo Zebrafish Model.
Tsea I, Olsen TK, Polychronopoulos PA, Tümmler C, et al · · 2024 · cited 4× · PMID 39766063 · DOI 10.3390/cancers16244162 -
BCOR mutations define a therapeutic vulnerability to DHODH Inhibition in acute myeloid leukemia.
Robert F, Badja C, Boushaki S, Degasperi A, et al · · 2026 · PMID 41549155 · DOI 10.1007/s00277-026-06773-z -
BCOR Mutations Define a Therapeutic Vulnerability to DHODH Inhibition in Acute Myeloid Leukemia
Robert F, Badja C, Boushaki S, Degasperi A, et al · · 2025 · DOI 10.21203/rs.3.rs-7470212/v1
Verify or expand the search:
- PubMed search for NCT03834584
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
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Other Agios Pharmaceuticals, Inc. trials
Trials by the same sponsor.
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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 NCT03834584 (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 Agios Pharmaceuticals, Inc.
- Last refreshed: 25 August 2020
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/NCT03834584.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing