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Tolizumab (anti-IL-6) in combination with nitazoxanide (anti-Wnt/ß-catenin) in the treatment of recurrent or surgical residual enamel cell-type craniopharyngiomas

Tolizumab (anti-IL-6) in combination with nitazoxanide (anti-Wnt/ß-catenin) in the treatment of recurrent or surgical residual enamel cell-type craniopharyngiomas

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108033
Enrollment
Unknown
Registered
2025-08-22
Start date
2025-08-22
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

Adamantinomatous craniopharyngioma (ACP)

Interventions

NTZ and tolizumab combination therapy:NTZ 500 mg orally, tolizumab 12 mg/kg intravenously
NTZ:NTZ 500 mg orally

Sponsors

FuJIan SanBo FuNeng Brain Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Twenty patients with recurrent or surgical residual ACP were recruited (criteria for evaluating the efficacy of solid tumours RECIST 1.1 evaluated on the basis of CT or MRI, with the longest diameter of the lesion being at least 10 mm); 2.Both men and women. 3.Age 3-60. 4.Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Accompanied by hydrocephalus; 2.Impaired consciousness exists; 3.SF-36 scale quantitative quality of life assessment parameters <50 points. 4.Unwillingness to comply with all procedures associated with the study, or failure to comply with protocol requirements, refusal to follow up or cooperate with examinations during the course of the study, entitles the party responsible for the study to suspend the subject without liability. 5.Those who are pregnant or plan to become pregnant within 1 year, breastfeeding women. 6.Those who were unable to cooperate with follow-up visits and did not have family members/carers who were able to attend and support all study visits during the consent process.

Design outcomes

Primary

MeasureTime frame
Imaging indicators;

Countries

China

Contacts

Public ContactZhixiong Lin

FuJIan SanBo FuNeng Brain Hospital

linzx@ccmu.edu.cn+86 591 63510010

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026