Imatinib
For an informed discussion with your doctor or pharmacist. This information collection is not a clinically validated interaction checker. Missing data do not establish safety. Do not change or stop prescribed medicines on the basis of this information. The findings apply to the specific conditions studied; laboratory and animal studies cannot be directly extrapolated to humans.
Active substance: Imatinib
Examples of brand names: Glivec [EU/DE]
ATC code: L01EA01
Main use (for orientation): CML; GIST
Documented research summary
Two preclinical CBD/imatinib combination papers recorded. No clinical pharmacokinetic interaction demonstrated; a laboratory antitumour effect is not a treatment recommendation.
Uncertainties and limitations
Single-ingredient oral imatinib preparation for human use, mesylate salt.
Shared enzymes must not be equated with clinical evidence of an interaction; CBD/THC findings cannot be extrapolated to other cannabinoids.
Separately recorded findings
2 separately recorded findings. Each statement applies to its documented study context.
CBD – laboratory and animal studies
Finding ID: B0178
Type of result: Preclinical evidence
Observation: Synergistic antiproliferative effect of CBD and imatinib in CML cells.
Mechanism: TRPV2/mitophagy and cellular differentiation
Study type: Cell and, where applicable, animal experiment; abstract assessed
Context studied: CML cell models, including imatinib-resistant cells; no patient pharmacokinetics.
Clinical interpretation: Experimental finding; no clinical treatment or dose recommendation
Limitations and uncertainties: Abstract-based; concentrations and combination effect sizes not extracted from the full text. A formal erratum (PMID37221079, 2023) replaces Figure 1B; consider the corrected presentation. This erratum is not a retraction notice.
Original sources for this finding: The effects of cannabidiol via TRPV2 channel in chronic myeloid leukemia cells and its combination with imatinib. [BMED34971020]; Correction: The effects of cannabidiol via TRPV2 channel in chronic myeloid leukemia cells and its combination with imatinib [AUDIT_B_CORR_37221079]
CBD – laboratory and animal studies
Finding ID: B0179
Type of result: Preclinical evidence
Observation: CBD plus imatinib enhanced apoptosis/differentiation-related signals in sensitive K-562S cells; resistant K-562R cells showed only partial restoration.
Mechanism: Exosomal miRNA signalling pathways
Study type: Cell and, where applicable, animal experiment; abstract assessed
Context studied: In-vitro transcriptomics/miRNA, not clinical evidence concerning resistance.
Clinical interpretation: Experimental finding; no clinical treatment or dose recommendation
Limitations and uncertainties: Biomarker/cell finding; no evidence of improved patient prognosis.
Original sources for this finding: Cannabidiol modulates exosomal miRNA networks to enhance Imatinib mesylate response in chronic myelogenous leukemia. [BMED41657764]
References and access status
[V2_LABEL_D0367] IMATINIB MESYLATE (IMATINIB) TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.]
Original source / bibliographic reference
Authors: Golden State Medical Supply, Inc.
Year: 2026
Source type: Official US SPL / DailyMed
Source access – 23 October 2026: Source destination was accessible when checked.
Bibliographic attribution or source identity cross-checked.
[BMED41657764] Cannabidiol modulates exosomal miRNA networks to enhance Imatinib mesylate response in chronic myelogenous leukemia.
Original source / bibliographic reference
Authors: Donchev PP, Vasileva EY, Paunova-Krasteva TS, Danova ST.
Year: 2026
Source type: Publication; title and abstract reviewed
DOI: 10.1016/j.gmg.2026.100094
PMID: 41657764
Source access – 23 October 2026: Automated direct retrieval was restricted; this does not establish that the link is broken.
Bibliographic attribution or source identity cross-checked.
PubMed – bibliographic reference / abstract
PubMed Central – archived text
DOI – publisher access (access restrictions may apply)
[BMED34971020] The effects of cannabidiol via TRPV2 channel in chronic myeloid leukemia cells and its combination with imatinib.
Original source / bibliographic reference
Authors: Maggi F, Morelli MB, Tomassoni D, Marinelli O, Aguzzi C, Zeppa L, Nabissi M, Santoni G, Amantini C.
Year: 2022
Source type: Publication; title and abstract reviewed
DOI: 10.1111/cas.15257
PMID: 34971020
Source access – 23 October 2026: Automated direct retrieval was restricted; this does not establish that the link is broken.
Bibliographic attribution or source identity cross-checked.
PubMed – bibliographic reference / abstract
PubMed Central – archived text
DOI – publisher access (access restrictions may apply)
[AUDIT_B_CORR_37221079] Correction: The effects of cannabidiol via TRPV2 channel in chronic myeloid leukemia cells and its combination with imatinib
Original source / bibliographic reference
Authors: Correction has no separately listed authors in PubMed; corrects Maggi et al.
Year: 2023
Source type: Published Erratum
DOI: 10.1111/cas.15825
PMID: 37221079
Source access – 23 October 2026: Automated direct retrieval was restricted; this does not establish that the link is broken.
Bibliographic attribution or source identity cross-checked.
PubMed – bibliographic reference / abstract
DOI – publisher access (access restrictions may apply)
Europe PMC – full-text access according to the literature database – Listed as freely available HTML full text in the official Europe PMC metadata. Direct retrieval was not fully verified here.
Research as of 23 October 2026. Not all original full texts could be reviewed in full. Source accessibility and the strength of scientific evidence must be assessed separately. An accessible link does not establish medical approval; a bibliographic record with an abstract does not replace the original full text.
Drug search and explanation of the evidence · Guide: cannabinoids and medicines · Author and responsibility
Imatinib and cannabinoids: documented findings, evidence, sources and data gaps. Research information for discussion with your doctor or pharmacist.
