ClinicalTrials.gg
Status unknownNCT05589961Updated Oct 21, 2022

Safety and Efficacy of TRPP Therapy in Glioblastoma Multiforme

An Early Phase 1 interventional study of TMZ in Glioblastoma Multiforme, sponsored by The Second Hospital of Hebei Medical University. Status unknown at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2022-10-21.

Sponsored by The Second Hospital of Hebei Medical University · Early Phase 1, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Oct 2022), so the status shown — last known as Recruiting — may be out of date.
Phase
Early Phase 1
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study summary

The primary objective of this study is to evaluate the safety of an innovative integrated treatment regimen for recurrent glioblastoma , including patients with recurrent glioblastoma multiforme.

Read the detailed description

This study is a single-center, prospective, open-label, single-arm clinical study of an innovative integrated treatment regimen for recurrent glioblastoma multiforme.

The main outcome measurement of the study is to evaluate the safety of the integrated treatment regimen for glioblastoma multiforme. Secondary outcome measurement are OS, PFS, ORR, and quality of life. Safety is evaluated by monitoring adverse events, physical examination results, vital signs, ECG, hematology, and clinical biochemistry. Imaging was performed at the end of every 3 sessions to assess treatment outcome and disease progression. The whole treatment and efficacy will be observed for two years.

02

Conditions studied

  • Glioblastoma Multiforme

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03

In context

Glioblastoma

2,132 studies on the registry are indexed under Glioblastoma; 464 are open to participants now.

This study's planned enrollment of 10 is below the median of 36 across 1,753 interventional studies indexed under Glioblastoma.

Browse Glioblastoma studies →

Lead sponsor

The Second Hospital of Hebei Medical University is the lead sponsor of 21 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • The pathological result of glioblastoma WHO grade 4;
  • Received standard TMZ chemotherapy and radiotherapy;
  • It is not suitable to undergo surgical resection of the lesion again or other drug treatment, or the patient refuses other treatment;
  • Men and women aged 18-75;
  • Disease progression was confirmed by CT or MRI examination within 4 weeks before enrollment;
  • score ≥70;
  • Expected survival time ≥ 3 months, and can meet the follow-up requirements;
  • Within 7 days before the start of treatment, the results of routine blood tests, liver and renal function tests, and hemagglutination laboratory tests meet the following criteria:

Leukocyte (WBC) ≥ 3.0×109/L

(PLT) ≥ 100×109/L

Neutrophil (ANC) ≥ 1.5×109/L

(HGB) ≥ 90g/L

Serum albumin ≥2.8g/dL

(AST) ≤2.5× (ULN) (\< 5×ULN for liver )

Alanine aminotransferase (ALT) ≤2.5×ULN (≤5×ULN for liver metastases)

Total (TIBC) ≤1.5×ULN, patients with liver cancer or liver metastases should ≤2×ULN

Serum creatinine (CR)≤1.5×ULN or ≥50ml/min

AST and ALT levels ≤ 2.5×ULN, and patients with liver metastases or liver cancer should ≤ 5×ULN

(INR) ≤ 1.5

Prothrombin time (PT) and activated partial thromboplastin time (APTT) ≤ 1.5×ULN

  • Pregnancy should be ruled out for fertile women, and HCG tests for early pregnancy must be negative; Both male and female participants should ensure that they use during the study and continue to use contraception until the end of the follow-up period;
  • Volunteer to participate in the clinical study, cooperate with the doctor to carry out the study, and sign the form.

Exclusion criteria

Exclusion Criteria:

  • Participating in another clinical trial;
  • Recurrence within 4 weeks after surgery;
  • Recurrence within 4 weeks after chemotherapy;
  • Recurrence within 4 weeks after radiotherapy;
  • Increased intracranial pressure: midline shift ≥5mm, visual edema, vomiting and nausea, or poor level of consciousness;
  • Have active infection that is not controlled with appropriate anti-infective therapy;
  • Patients with mental illness or other conditions, such as uncontrollable heart disease or lung disease, diabetes, etc., cannot comply with the requirements of research treatment and monitoring;
  • Organ transplants;
  • Pregnant or lactating women; Persons with disabilities (blind, deaf, dumb, mentally disabled, physically disabled) or suffering from mental diseases as prescribed by law; Drug users or patients with a history of adverse drug abuse and alcohol dependence within 5 years;
  • (HIV) infection or known acquired immunodeficiency syndrome (AIDS), untreated active hepatitis (, defined as a positive hepatitis B surface antigen [HBsAg] test, HBV-DNA ≥ 500 IU/ml and abnormal liver function; , defined as hepatitis C antibody [HCV-AB] positive, HCV-RNA above the detection limit of the assay, and abnormal liver function) or co-infection with hepatitis B and C;
  • Any other factors that the investigator deems inappropriate for the subject to participate in the study.
Terms in these criteria, in plain language(15)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Karnofsky performance status (KPS)

A 0–100 scale of how well someone can carry out everyday activities. 100 is no complaints and no signs of illness; 70 is able to look after yourself but not to work or keep up normal activity; 50 is needing considerable help and frequent medical care.

Studies often ask for 60 or 70 and above. Your doctor gives the score.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

Bilirubin

A yellow substance made when red blood cells are broken down, which the liver clears. A high level can mean a problem with the liver or the bile ducts.

Criteria often allow more for people with Gilbert’s syndrome, a harmless inherited condition that raises bilirubin.

Creatinine clearance (CrCl)

How quickly the kidneys clear creatinine, a waste product, from the blood. A study may estimate it from a blood test with age, weight and sex (often by the Cockcroft–Gault formula), or measure it using blood and urine collected over a set time. Given in mL/min; higher is better.

INR, PT and aPTT (clotting tests)

Blood tests of how long blood takes to clot. The INR is the prothrombin time (PT) put on a common scale; about 1 is usual for someone not taking a blood thinner.

Criteria often make an exception for people on a blood thinner such as warfarin, whose INR is raised on purpose.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

05

Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Experimental
    integrated treatment regimen(TRPP)

    Drug: TMZ

Interventions

  • DrugTMZ

    After enrollment, temozolomide 50mg/m2 was given orally for QD until progression, and radiotherapy and PF 0.2g/ time for TID were started one week later until progression. Pembrolizumab 200mg once every 3 weeks until progression; The radiotherapy regimen depends on the patient's recurrence and initial treatment.

    Also known as: PD-1, RF

This study also gives Pembrolizumab. No intervention listed here names it: that was found by reading the record.

06

What researchers measure

Primary outcomes

  1. To Evaluate the Safety of the Integrated Treatment Regimen for Glioblastoma Multiforme

    Evaluating the possible adverse reactions recorded are analyzed, mainly including the number, incidence and severity of radiochemotherapy-related adverse reactions and immune-related adverse reactions (irAE) from the beginning of treatment to the progression of disease. Include: 1. Systemic reaction: such as dizziness, fatigue, bone or muscle pain, etc.; 2. drug allergic reaction; 3. Cytopenia caused by myelosuppression may lead to severe infection, bleeding, anemia, etc.; 4. Gastrointestinal symptoms such as loss of appetite, nausea, vomiting, abdominal pain, diarrhea, constipation, fecal occult blood, gastrointestinal bleeding, etc.; 5. Immune-related adverse reactions (irAE) : Pneumonia, including immune correlation immunity correlation colitis, correlation immune correlation hepatitis, nephritis, immune related endocrine diseases, immune correlation skin reactions and other immune system Related adverse reactions.

    Time frame: From first dose until 30 days after the last dose (up to approximately 2 years ) (Cycle length= 21 days)

Secondary outcomes

  1. To Evaluate the survival of the Integrated Treatment Regimen for Glioblastoma Multiforme

    Using the RANO criteria as the efficacy evaluation criteria, multimodal MRI and 11C-MET PET/CT examination were performed to distinguish false progression, recurrence and radiation injury if necessary. MDT was discussed when necessary. OS:Survival was measured from the start of treatment for 2 years or until death (from any cause within 2 years). Overall survival was estimated by planMeier. Patients who are still alive will be examined at the last contact visit. See RANO Standard for specific standards.

    Time frame: From first dose until 30 days after the last dose (up to approximately 2 years ) (Cycle length= 63 days)

  2. To Evaluate the efficacy of the Integrated Treatment Regimen for Glioblastoma Multiforme

    Using the RANO criteria as the efficacy evaluation criteria, multimodal MRI and 11C-MET PET/CT examination were performed to distinguish false progression, recurrence and radiation injury if necessary. MDT was discussed when necessary. PFS:Progression-free survival (PFS) was calculated from the date of SD after treatment until the first occurrence of disease progression. Progression-free survival was estimated by Haplan-Meier. Patients who are still alive and have no disease progression will be examined at the last visit/contact. Whether disease progression is due to the primary or metastases should be documented.ORR and quality of life. See RANO Standard for specific standards.

    Time frame: From first dose until 30 days after the last dose (up to approximately 2 years ) (Cycle length= 63 days)

07

Study locations

1 of 1 sites recruiting
  • the Second Hospital of HeBei Medical University
    Shijia Zhuang, Hebei, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 21, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05589961
Lead sponsor
The Second Hospital of Hebei Medical University
Responsible party
Sponsor
First posted
Oct 21, 2022
Start date
Oct 2022 (estimated)
Primary completion
Jul 2024 (estimated)
Completion
Jul 2024 (estimated)
Last update
Oct 21, 2022

Study contacts

Chunyan Li, Academician
Contact
hebeichunyanli@aliyun.com
0311-87064024
Chunyan Li, Academician
study chair · The Second Hospital of Hebei Medical University

Oversight

FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2022. You cannot join it, but the record below documents what was studied.

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Studies of the drugs tested here: Temozolomide · Pembrolizumab

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