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Nk Cell Therapy for Recurrent Glioblastoma Multiform Patients

The Safety Evaluation of Ex Vivo Activated Haploidentical Natural Killer Cells (NK) in Recurrent Glioblastoma Multiform Patients (Clinical Trial Phase I)

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05108012
Enrollment
5
Registered
2021-11-04
Start date
2021-08-01
Completion date
2022-04-30
Last updated
2021-11-22

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

Conditions

Glioblastoma Multiform, Recurrent Glioblastoma

Keywords

Natural Killer Cells (NK), Glioblastoma Multiform (GBM)

Brief summary

Glioblastoma multiform is one of the most invasive and deadly cancers that progresses rapidly and leads to death. Surgery with radiotherapy /chemotherapy, as a treatment approach is ineffective in some cases and is associated with relapse and death. Immunotherapy is a special strategy that used as an adjunct therapy in various cancers and among the various methods of immunotherapy; it seems that cell therapy with NK cells is of special importance. A previous study conducted at the Royan Research Institute showed that NK cell proliferation and amplification resulted in the removal of glioblastoma tumor masses in the animal model. The animals had no evidence of tumor recurrence after treatment, and all tumor-related complications resolved after treatment. Therefore, in this study, the investigators intend to evaluate the safety of ex vivo activated cells in 5 patients with glioblastoma multiform whose disease has returned after treatment and who have not had any appropriate treatment.

Detailed description

1- patient selection 2- leukapheresis 3- CD56+ cells isolation 4- NK cells activation 5- assessment of functionality and purity 6- quality control tests 7-NK cell injection in tumor cavity.

Interventions

BIOLOGICALNK cell therapy

Activated NK cell injection in tumor cavity of patient with GBM (Glioblastoma Multiform)

Sponsors

Tehran University of Medical Sciences
CollaboratorOTHER
Royan Institute
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The investigators will enroll 5 patients (3-60 year, both sex, -Lansky performance scale/Karnofsky performance scale: 70-100%) with recurrent Glioblastoma Multiform. A haploidentical donor will enter for each patient.

Eligibility

Sex/Gender
ALL
Age
3 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Age: 3-60 Year - * Sex: Both * Lansky performance scale/Karnofsky performance scale: 70-100% * Life span expectation: \>6 months * Hemoglobin: \> 10.0 g/dl * Platelet count \> 100,000/mm³ * Serum total bilirubin \< 1.5 times upper limit of normal (ULN) * ALT and AST \< 2.5 times ULN * Serum creatinine \< 1.5 times ULN * No diagnosis of any other invasive cancer within the past 5 years. * No concurrent serious medical or psychiatric illness that may interfere with giving informed consent or conducting this study

Exclusion criteria

* Patients whose MRI and MRS images is in favor of radio necrosis. * Due to emergency conditions, the patient cannot tolerate the new treatment * Lack of a suitable donor or insufficient number of NK cells. * Development of a new neurological defect after the first injection * Patient death during surgery * Closing the reservoir for the next injection (if this problem is resolved, the injections will be done again).

Design outcomes

Primary

MeasureTime frameDescription
Toxicity assay4 weeks of last injectionToxicity as assessed by NCI CTCAE version 3.0
Adverse Events (AEs)1 yearDefined as the number and severity of adverse events
Safety evaluationFrom injection time point up to 48 hoursSafety evaluated by assessing the medical symptoms measurement: Fever, Hysteria and Convulsion
MRI and MRS from the tumor region1 months after last dose of NK cell injection up to 1 year each 3 monthsDefined tumoral residua and tumor cell recurrence

Secondary

MeasureTime frameDescription
Patient survivalAfter surgery up to an average of 1 yearEvaluation of patient's life extension followed by NK cell therapy

Countries

Iran

Contacts

Primary ContactMarzieh Ebrahimi, PhD
marzieh.ebrahimi@gmail.com;mebrahimi@royan-rc.ac.ir+98 21 235 62516
Backup ContactZohreh Habibi, M.D
z-habibi@gmail.com+98 912 336 5598

Outcome results

None listed

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