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Clinical Trial Details — Status: Available

Administrative data

NCT number NCT05974410
Other study ID # AVM0703-EAP
Secondary ID
Status Available
Phase
First received
Last updated

Study information

Verified date July 2023
Source AVM Biotechnology Inc
Contact Mia Lor
Phone 12062607770
Email mlor@avmbiotech.com
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

AVM Biotechnology, Inc., provides immunomodulatory AVM0703 to solid tumor and blood cancer patients upon request by a US licensed MD or DO. As of July 2023, 22 patients have been treated through this FDA-EAP including patients diagnosed with relapsed or recurring glioblastoma, inoperable/chemotherapy ineligible CNS Squamous Cell Carcinoma, metastatic Breast Cancer, ovarian cancer, gastric cancer, Hodgkin's Lymphoma, Mixed Phenotype Acute Myelogenous Leukemia, colon cancer, B-ALL, Malignant Myxoid Spindle Cell Neoplasm, non-small cell lung cancer, DLBCL with CNS involvement, metastatic prostate cancer, Anaplastic T-cell Non-Hodgkin's Lymphoma.


Recruitment information / eligibility

Status Available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Exclusion Criteria: -

Study Design


Intervention

Drug:
AVM0703
small molecule immunomodulatory drug
Hydrocortisone
physiologic circadian glucocorticoid
Proton pump inhibitor


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
AVM Biotechnology Inc
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