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NCT04502706
Study of GS-0189 (Formerly FSI-189) as Monotherapy and in Combination With Rituximab in Participants With Relapsed/Refractory Non-Hodgkin Lymphoma
Phase 1 trial testing GS-0189 in Non-hodgkin Lymphoma in 9 participants. Terminated before completion.
31 March 2022
Quick facts
| Lead sponsor | Gilead Sciences |
|---|---|
| Phase | Phase 1 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | sequential |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 9 |
| Start date | 17 November 2020 |
| Primary completion | 31 March 2022 |
| Estimated completion | 31 March 2022 |
| Sites | 5 locations across United States |
Drugs / interventions tested
Conditions studied
- Non-hodgkin Lymphoma — all drugs for Non-hodgkin Lymphoma →
Sponsor
Gilead Sciences — full company profile →
Who can join
18 and older, any sex, with Non-hodgkin Lymphoma. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The primary objective of this study is to determine the safety and tolerability of GS-0189 (formerly FSI-189) as monotherapy and in combination with rituximab in participants with relapsed/refractory (R/R) non-Hodgkin lymphoma (NHL).
Publications & conference data
8 peer-reviewed publications reference this trial (live from Europe PMC):
-
Targeting macrophages in cancer immunotherapy.
Duan Z, Luo Y. · · 2021 · cited 462× · PMID 33767177 · DOI 10.1038/s41392-021-00506-6 -
Tissue macrophages: origin, heterogenity, biological functions, diseases and therapeutic targets.
Guan F, Wang R, Yi Z, Luo P, et al · · 2025 · cited 155× · PMID 40055311 · DOI 10.1038/s41392-025-02124-y -
CD47-SIRPα-targeted therapeutics: status and prospects.
Maute R, Xu J, Weissman IL. · · 2022 · cited 105× · PMID 35754851 · DOI 10.1016/j.iotech.2022.100070 -
Targeting the tumor microenvironment in B-cell lymphoma: challenges and opportunities.
Liu Y, Zhou X, Wang X. · · 2021 · cited 98× · PMID 34404434 · DOI 10.1186/s13045-021-01134-x -
CD47-SIRPα axis blockade in NASH promotes necroptotic hepatocyte clearance by liver macrophages and decreases hepatic fibrosis.
Shi H, Wang X, Li F, Gerlach BD, et al · · 2022 · cited 71× · PMID 36417485 · DOI 10.1126/scitranslmed.abp8309 -
Targeting CD47/SIRPα as a therapeutic strategy, where we are and where we are headed.
Qu T, Li B, Wang Y. · · 2022 · cited 66× · PMID 35418166 · DOI 10.1186/s40364-022-00373-5 -
Progress of CD47 immune checkpoint blockade agents in anticancer therapy: a hematotoxic perspective.
Chen YC, Shi W, Shi JJ, Lu JJ. · · 2022 · cited 50× · PMID 34609596 · DOI 10.1007/s00432-021-03815-z -
Cancer Therapy Targeting CD47/SIRPα.
Dizman N, Buchbinder EI. · · 2021 · cited 41× · PMID 34944850 · DOI 10.3390/cancers13246229
Verify or expand the search:
- PubMed search for NCT04502706
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Other Gilead Sciences trials
Trials by the same sponsor.
- NCT07115368 — Study of GS-1219 in Participants With HIV-1 · Phase 1 · terminated
- NCT06784973 — Study of Obeldesivir to Treat Children With Respiratory Syncytial Virus (RSV) Infection · Phase 2 · terminated
- NCT06683482 — A Qualitative Study on Advanced Breast Cancer Patients and Their Caregivers in Spain · completed
- NCT06613685 — Study of Oral Weekly GS-1720 and GS-4182 Compared With Biktarvy in People With HIV-1 Who Have Not Been Treated · Phase 2, PHASE3 · terminated
- NCT06585150 — Study of Obeldesivir to Treat Nonhospitalized Adults With Acute Respiratory Syncytial Virus (RSV) Infection · Phase 2 · terminated
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 NCT04502706 (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 Gilead Sciences
- Last refreshed: 5 June 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/NCT04502706.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing