A Phase I-c Study of Recombinant GM-CSF Herpes Simplex Virus to TreatⅣ M1c
NCT ID: NCT03048253
Last Updated: 2017-10-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
30 participants
OBSERVATIONAL
2016-03-29
2019-10-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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OrienX010
Beijing biological technology co., LTD. Research and development of the source and force of recombinant human GM-CSF herpes simplex virus injection (OrienX010), is a genetically engineered type 1 herpes simplex virus (HSV - 1) as the carrier insert GM-CSF gene therapy drug.Its carrier is made of isolated from patients with oral Chinese wild single blister virus type I (CL1), after gene recombination technology successively removing ICP34.5, ICP47 and insert the deactivation ICP6 gene, and at the site of the original ICP34.5 insert guided by IE promoter of hCMV human GM-CSF gene.
Eligibility Criteria
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Inclusion Criteria
* General physical status score (ECOG) 0-2 points
* Lifetime is expected to more than 4 months
* Always anti-tumor treatment (including/radiation therapy, immune therapy, targeted therapy, endocrine therapy, etc.) to end more than 4 weeks (using the nitroso urea class and mitomycin chemotherapy drug withdrawal over 6 weeks), and always treat the adverse reaction of restored or stability
Exclusion Criteria
* In group of four weeks before received the treatment of herpes simplex virus, such as acyclovir, ganciclovir, respectively.there is galloway, vidarabine, etc
* In group of four weeks before too much surgery
* Screening stage HSV - 1 antibody IgG and IgM are negative
18 Years
ALL
No
Sponsors
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OrienGene Biotechnology Ltd.
INDUSTRY
Responsible Party
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Locations
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Beijing cancer hospital
Beijing, Beijing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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OrienX010-II-10
Identifier Type: -
Identifier Source: org_study_id