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NCT03588936
Nivolumab and Tocilizumab for Relapsed Hematological Malignancy Post-allogeneic Transplant
Phase 1 trial testing Nivolumab (.25 mg/kg) in Acute Leukemia in 2 participants. Terminated before completion.
15 July 2020
Quick facts
| Lead sponsor | Medical College of Wisconsin |
|---|---|
| Phase | Phase 1 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | sequential |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 2 |
| Start date | 14 September 2018 |
| Primary completion | 15 July 2020 |
| Estimated completion | 15 July 2020 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Nivolumab (.25 mg/kg) — full drug profile →
- Tocilizumab (tocilizumab) — full drug profile →
- Nivolumab (.5 mg/kg) — full drug profile →
Conditions studied
- Acute Leukemia — all drugs for Acute Leukemia →
- Chronic Leukemia — all drugs for Chronic Leukemia →
- Lymphoma — all drugs for Lymphoma →
- Myelodysplastic Syndromes — all drugs for Myelodysplastic Syndromes →
Sponsor
Medical College of Wisconsin
Who can join
18 and older, any sex, with Acute Leukemia or Chronic Leukemia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is a phase 1, interventional single arm, open label, treatment study designed to evaluate the safety combination programmed cell death protein 1 (PD-1) and interleukin 6 (IL-6) inhibition in participants with relapsed disease post-allogeneic transplant.
Publications & conference data
6 peer-reviewed publications reference this trial (live from Europe PMC):
-
Targeting cytokine and chemokine signaling pathways for cancer therapy.
Yi M, Li T, Niu M, Zhang H, et al · · 2024 · cited 264× · PMID 39034318 · DOI 10.1038/s41392-024-01868-3 -
Landscape of Myeloid-derived Suppressor Cell in Tumor Immunotherapy.
Hao Z, Li R, Wang Y, Li S, et al · · 2021 · cited 72× · PMID 34689842 · DOI 10.1186/s40364-021-00333-5 -
Novel agents targeting leukemia cells and immune microenvironment for prevention and treatment of relapse of acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation.
Shi W, Jin W, Xia L, Hu Y. · · 2020 · cited 15× · PMID 32837873 · DOI 10.1016/j.apsb.2020.06.012 -
The Role of Immune Checkpoints after Cellular Therapy.
Schmitz F, Wolf D, Holderried TAW. · · 2020 · cited 13× · PMID 32455836 · DOI 10.3390/ijms21103650 -
Dual efficacy of tocilizumab in managing PD-1 inhibitors-induced myocardial inflammatory injury and suppressing tumor growth with PD-1 inhibitors: a preclinical study.
Chen Y, Luo Y, Liu Y, Luo D, et al · · 2025 · cited 7× · PMID 39752010 · DOI 10.1007/s00262-024-03899-9 -
Is It Possible to Separate the Graft-Versus-Leukemia (GVL) Effect Against B Cell Acute Lymphoblastic Leukemia From Graft-Versus-Host Disease (GVHD) After Hematopoietic Cell Transplant?
Rozmus J, Bhatt ST, Buxbaum NP, Cuvelier GDE, et al · · 2022 · cited 4× · PMID 35402356 · DOI 10.3389/fped.2022.796994
Verify or expand the search:
- PubMed search for NCT03588936
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Medical College of Wisconsin 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 NCT03588936 (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 Medical College of Wisconsin
- Last refreshed: 11 October 2021
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/NCT03588936.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing