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This study is an extension of evaluation of the surgical resection arm, Arm B, from a phase Ib study in which dose escalation on arm B was completed.

Single dose of 3x10e11 vector particles of CAN-2409 delivered to the tumor bed after resection on day 0.

CAN-2409

Single course of valacyclovir at dose of 2 grams orally three times per day for 14 days starting on day 1-3

Concomitant TMZ will be administered orally once a day at a dose of 75 mg/m2 starting the next day after completing prodrug and continued for 6 weeks. Adjuvant TMZ will be administered days 1 to 5 of a 28-day cycle for 6 cycles with 150 mg/m2 administered for cycle 1, and 150 to 200 mg/m2 administered for cycles 2 to 6. Adjuvant treatment will start 1 month following completing RT.

Radiation will be administered to up-front patients as per standard of care for the patient. It will start 3-7 days after CAN-2409 injection, preferably closer to 3 days. It will consist of standard external field radiation, limited to the area of tumor and brain adjacent to tumor, fractionated at doses of 200cGy per day for approximately 6 weeks to a total of 5500-6000 cGy.

Radiation therapy

E. Antonio Chiocca, MD, PhD

The purpose of this study was to evaluate the safety and potential efficacy of CAN-2409 (also known / previously described as AdV-tk, GMCI) for malignant gliomas. The approach used an adenoviral vector (disabled virus) engineered to express the Herpes thymidine kinase gene (aglatimagene besadenovec, CAN-2409), followed by an antiherpetic prodrug, valacyclovir. CAN-2409 was injected into the resection bed after standard tumor surgery and valacyclovir pills were taken for 14 days. Standard radiation and chemotherapy were administered which have been shown to work cooperatively with CAN-2409 + prodrug to kill tumor cells. The hypothesis is that this combination therapy can be safely delivered and will lead to improvement in the clinical outcome for patients with newly diagnosed malignant gliomas, including glioblastoma multiforme (WHO grade IV) and anaplastic astrocytomas (WHO grade III).

Patients had resectable or partially resectable malignant glioma and received injection of CAN-2409 into remaining tumor or tumor bed after resection. Pathologic confirmation of malignant glioma must be made prior to CAN-2409 injection; if this was not possible, the injection was not performed and the subject was no longer eligible for the study. The oral prodrug, valacyclovir, started 1-3 days after CAN-2409 injection and continued for 14 days. Standard radiotherapy began on average 7 days after CAN-2409 injection for the up-front course. Patients received temozolomide as per standard of care after completion of prodrug.

Phase 2a Study of CAN-2409 With Standard Radiation Therapy for Malignant Glioma

A Phase IIa Study of AdV-tk + Valacyclovir Gene Therapy in Combination With Standard Radiation Therapy for Malignant Gliomas

Candel Therapeutics, Inc.

This study is an extension of evaluation of the surgical resection arm, Arm B, from a phase Ib study in which dose escalation on arm B was completed.

CAN-2409: Single dose of 3x10e11 vector particles of CAN-2409 delivered to the tumor bed after resection on day 0.

Valacyclovir: Single course of valacyclovir at dose of 2 grams orally three times per day for 14 days starting on day 1-3

Temozolomide: Concomitant TMZ will be administered orally once a day at a dose of 75 mg/m2 starting the next day after completing prodrug and continued for 6 weeks. Adjuvant TMZ will be administered days 1 to 5 of a 28-day cycle for 6 cycles with 150 mg/m2 administered for cycle 1, and 150 to 200 mg/m2 administered for cycles 2 to 6. Adjuvant treatment will start 1 month following completing RT.

Radiation therapy: Radiation will be administered to up-front patients as per standard of care for the patient. It will start 3-7 days after CAN-2409 injection, preferably closer to 3 days. It will consist of standard external field radiation, limited to the area of tumor and brain adjacent to tumor, fractionated at doses of 200cGy per day for approximately 6 weeks to a total of 5500-6000 cGy.

Single Arm

9 patients were withdrawn from the study prior to receiving treatment due to pathology inconsistent with malignant glioma.

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization	Link
Phase 2a Study of CAN-2409 With Standard Radiation Therapy for Malignant Glioma	NCT00589875	Malignant Gliom... Glioblastoma Mu... Anaplastic Astr... High Grade Glio...	CAN-2409 Valacyclovir Temozolomide Radiation thera...	18 Years -	Candel Therapeutics, Inc.
Phase 2a Study of CAN-2409 With Standard Radiation Therapy for Malignant Glioma	NCT00589875	Malignant Gliom... Glioblastoma Mu... Anaplastic Astr... High Grade Glio...	CAN-2409 Valacyclovir Temozolomide Radiation thera...	18 Years -	Candel Therapeutics, Inc.

Spots Global Cancer Trial Database for candel therapeutics, inc.