This small-size patient population expanded access program is to provide access toinvestigational product RZ-001 for up to around 4 patients with human telomerase reversetranscriptase(hTERT)-positive Glioblastoma (GBM) who are not eligible to participate inthe RZ-001-201 clinical study or in any other study involving the use of RZ-001
This expanded access protocol provides expanded access to RZ-001 to patients with
glioblastoma. After provision of written informed consent, subjects will be evaluated for
eligibility during the Screening period, a period of 28 days prior to the RZ-001
administration on Day 1. Subjects will then undergo treatment, 8 weeks of follow-up, and
bimonthly or quarterly (after 6 months from RZ-001 administration) survival follow-up.
Drug: RZ-001
Participants will receive a single intracerebral injection of RZ-001, Recombinant
adenovirus harboring the modified ribozyme construct with HSV-tk as a therapeutic
transgene
Inclusion Criteria:
1. Males and females legally considered to be adults in the country in which they are
participating in the study.
2. Histologically-confirmed Grade 4 astrocytoma, GBM, per The 2021 WHO Classification
of central nervous system (CNS) Tumors.
3. Recurrent GBM with radiographic evidence of the PD (progressive disease) which
contains measurable disease (≥ 1 cm bidirectional diameters) by contrast-enhancement
on MRI, as defined by the mRANO (modified Response Assessment in Neuro-Oncology)
criteria. Only localized unifocal or multifocal recurrence is allowed, while other
type of recurrences such as intraventricular, diffuse recurrence are not allowed.
Exclusion Criteria:
1. Diagnosis of other malignant tumors within 5 years prior to RZ-001 administration.
2. Have received chemotherapy within 4 weeks, and/or immunomodulatory therapy,
immunotherapy, antibody therapy, gene vector therapy, vaccine therapy, and/or matrix
metalloprotease inhibitor(s) within 3 months from Screening.
3. Have received radiotherapy within 12 weeks from Screening.
4. Have extracranial metastases of the tumor cells.
5. The subject is eligible for participation in any ongoing clinical study with RZ-001,
or has already received RZ-001 in the past.
6. The subject is being transferred from an ongoing clinical study for which they are
still eligible.
Brigham & Women's Hospital
Boston, Massachusetts, United States
Rznomics
+82-31-706-8730
rznomics@rznomics.com
Not Provided