Last reviewed · How we verify

NCT04502706

Study of GS-0189 (Formerly FSI-189) as Monotherapy and in Combination With Rituximab in Participants With Relapsed/Refractory Non-Hodgkin Lymphoma

Terminated Phase 1 Last updated 5 June 2023
What this trial tests

Phase 1 trial testing GS-0189 in Non-hodgkin Lymphoma in 9 participants. Terminated before completion.

Timeline
17 November 2020
Primary endpoint
31 March 2022
31 March 2022

Quick facts

Lead sponsorGilead Sciences
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment9
Start date17 November 2020
Primary completion31 March 2022
Estimated completion31 March 2022
Sites5 locations across United States

Drugs / interventions tested

Conditions studied

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):

  1. Targeting macrophages in cancer immunotherapy.
    Duan Z, Luo Y. · · 2021 · cited 462× · PMID 33767177 · DOI 10.1038/s41392-021-00506-6
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. Cancer Therapy Targeting CD47/SIRPα.
    Dizman N, Buchbinder EI. · · 2021 · cited 41× · PMID 34944850 · DOI 10.3390/cancers13246229

Verify or expand the search:

Other recruiting trials for Non-hodgkin Lymphoma

Currently open trials in the same condition.

Other Gilead Sciences trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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