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NCT04117958
Study of AMG 199 in Subjects With MUC17-Positive Solid Tumors Including Gastric, Gastroesophageal Junction, Colorectal, and Pancreatic Cancers
Phase 1 trial testing AMG 199 in MUC17-positive Solid Tumors in 58 participants. Terminated before completion.
1 June 2023
Quick facts
| Lead sponsor | Amgen |
|---|---|
| Phase | Phase 1 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | sequential |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 58 |
| Start date | 20 January 2020 |
| Primary completion | 1 June 2023 |
| Estimated completion | 1 June 2023 |
| Sites | 21 locations across France, Japan, Netherlands, Austria, Taiwan, Germany, South Korea, United States |
Drugs / interventions tested
- AMG 199 — full drug profile →
Conditions studied
- MUC17-positive Solid Tumors — all drugs for MUC17-positive Solid Tumors →
Sponsor
Amgen — full company profile →
Who can join
Adults 18 to 99, any sex, with MUC17-positive Solid Tumors. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
To evaluate the safety and tolerability of AMG 199 in adult subjects and to determine the maximum tolerated dose (MTD) and/or recommended phase 2 dose (RP2D).
Publications & conference data
8 peer-reviewed publications reference this trial (live from Europe PMC):
-
Signaling pathways and therapeutic interventions in gastric cancer.
Lei ZN, Teng QX, Tian Q, Chen W, et al · · 2022 · cited 220× · PMID 36209270 · DOI 10.1038/s41392-022-01190-w -
The landscape of bispecific T cell engager in cancer treatment.
Zhou S, Liu M, Ren F, Meng X, et al · · 2021 · cited 172× · PMID 34039409 · DOI 10.1186/s40364-021-00294-9 -
Current landscape and future directions of bispecific antibodies in cancer immunotherapy.
Wei J, Yang Y, Wang G, Liu M. · · 2022 · cited 127× · PMID 36389699 · DOI 10.3389/fimmu.2022.1035276 -
Overcoming Challenges for CD3-Bispecific Antibody Therapy in Solid Tumors.
Middelburg J, Kemper K, Engelberts P, Labrijn AF, et al · · 2021 · cited 122× · PMID 33466732 · DOI 10.3390/cancers13020287 -
Overcoming the challenges associated with CD3+ T-cell redirection in cancer.
Singh A, Dees S, Grewal IS. · · 2021 · cited 82× · PMID 33469153 · DOI 10.1038/s41416-020-01225-5 -
Overcoming cold tumors: a combination strategy of immune checkpoint inhibitors.
Ouyang P, Wang L, Wu J, Tian Y, et al · · 2024 · cited 66× · PMID 38545114 · DOI 10.3389/fimmu.2024.1344272 -
Bispecific antibodies in cancer therapy: Target selection and regulatory requirements.
Sun Y, Yu X, Wang X, Yuan K, et al · · 2023 · cited 62× · PMID 37719370 · DOI 10.1016/j.apsb.2023.05.023 -
Mucin1 and Mucin16: Therapeutic Targets for Cancer Therapy.
Lee DH, Choi S, Park Y, Jin HS. · · 2021 · cited 53× · PMID 34681277 · DOI 10.3390/ph14101053
Verify or expand the search:
- PubMed search for NCT04117958
- 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 NCT04117958 (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 Amgen
- Last refreshed: 14 October 2025
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/NCT04117958.
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