OncoMatch

OncoMatch/Clinical Trials/NCT05278715

Modified CV Regimen in Optic Pathway Glioma

Is NCT05278715 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Carboplatin and Vincristine for optic glioma.

Phase 2RecruitingBeijing Sanbo Brain HospitalNCT05278715Data as of Jun 2026Location: China

Treatment: Carboplatin · Vincristine · Recombinant human endostatinOptic pathway glioma (OPG) can result in visual deterioration. Symptomatic patients often report deficits in visual acuity (VA), visual field, visual-evoked potentials (VEPs), strabismus, proptosis, disc swelling, and other visual/neurological problems. VA itself remains one of the most important outcome measures for OPG patients, with various studies showing strong ties of VA level to overall quality of life and well-being . Maintenance of favorable VA and vision outcomes is of paramount importance in the management of OPG. In terms of management of OPG, surgery and radiotherapy are used on a more limited basis because of location of the tumors and risk of secondary tumors, respectively. Tumor stabilization often prioritized, and chemotherapy is considered ideal for tumor stabilization in OPG, but vision is not always retained and may worsen in some cases, partially due to low radiographic efficacy and long time interval to response of the current chemotherapy regimen. In the prior study, the investigators modified the traditional carboplatin combined with vincristine regimen by increasing the dose of carboplatin and combining with an anti-angiogenic drug. Of the 15 OPG patients, objective response rate was 80% and the time to response was only 3.3 months. 8 (53%) patients experienced an improvement in visual acuity during therapy and 6 (40%) were stable, which was higher than the historical studies. This study was launched to further verify the clinical efficacy of the modified regimen and its effect on visual acuity improvement.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Chemotherapy

CarboplatinVincristine

Other

Recombinant human endostatin

Cancer type

Glioblastoma

Biomarker criteria

Excluded: H3F3A (H3 K27M) H3K27 mutation

H3K27 mutations, even histopathological grade 1/2

Demographics

Ages 0–21

Prior therapy

Cannot have received: investigational agent

Lab requirements

Cardiac function

No dysfunction of major organs; Suffering from serious cardiovascular disease; T wave inversion or elevation or ST segment changes [excluded]

No dysfunction of major organs. Suffering from serious cardiovascular disease; T wave inversion or elevation or ST segment changes [excluded]

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT05278715 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior investigational agent disqualifies patients from enrollment.

Are patients with H3F3A alterations eligible?

No. H3F3A H3K27 mutation is an exclusion criterion.

Is there an age limit?

Yes. Patients must be 21 years or younger and at least 0 years old.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify

Related pages

Glioblastoma trials