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Preclinical Project on the Traitment of Acute Lymphoblastique Leukemia With NVP-BEP800, an Inhibitor of the Heat Shock Protein HSP90

Preclinical Project on the Traitment of Acute Lymphoblastique Leukemia With NVP-BEP800, an Inhibitor of the Heat Shock Protein HSP90

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04437420
Acronym
HSP-HEMATO
Enrollment
44
Registered
2020-06-18
Start date
2019-11-01
Completion date
2021-09-30
Last updated
2020-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute B Lymphoblastic Leukemia (B-ALL), Acute T Lymphoblastic Leukemia (T-ALL)

Brief summary

NVP-BEP800, a new HSP90 inhibitor, has particularly interesting therapeutic potential and represents hope in cancer pathologies. While it is currently being tested for solid cancers, no preclinical study has yet demonstrated its effectiveness in acute lymphoblastique leukemia (ALL). The investigators wish to study the effects of NVP-BEP800 on two different types of ALL (T and B-ALL).

Interventions

DRUGinjection of BEP 800

injection of BEP 800

OTHERControl

no injection of BEP 800

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patient suffering from acute lymphoblastic leukaemia whose biological samples are kept at the Biology Technical Platform.

Exclusion criteria

* Patient over 80 years of age

Design outcomes

Primary

MeasureTime frameDescription
Viability on primary ALL samples2 yearsThe effect of BEP-800 after 48 hours of treatment on T-ALL and B-ALL will be evaluated by counting viable cells by flow cytometry with a viability marker and specific antibodies to detect leukemia cells.

Secondary

MeasureTime frameDescription
Effect on SRC phosphorylation2 yearsThe effect of BEP-800 on T-ALL and B-ALL will be evaluated by flow cytometry by measuring HSP90 and SRC (phosphorylated), by intracellular labeling after permeabilization of the cells, 18 hours after treatment with BEP-800.

Countries

France

Contacts

Primary ContactFrançois GIRODON
francois.girodon@chu-dijon.fr0380295710

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026