Intrathecal Drug Delivery

2

Review clinical trials related to Intrathecal Drug Delivery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Intrathecal Therapy Versus Standard Care for Severe Cancer Pain

Approximately 66% of patients with advanced cancer experience pain, which is often inadequately controlled and associated with a decline in health-related quality of life (HRQoL). Conventional pharmacologic management, ranging from simple analgesics to strong opioids, is frequently limited by insufficient efficacy and systemic side effects. Intrathecal drug delivery (IDD) offers targeted, continuous medication infusion directly into the intrathecal space, allowing lower systemic doses and potentially reducing side effects while maintaining effective analgesia. The CAREGIVER study is a randomized, controlled trial designed to evaluate whether patients with severe refractory cancer pain receiving IDD experience a difference in HRQoL compared to those receiving conventional medical management (CMM) with oral pain medications.

Participants needed: 72
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Universitair Ziekenhuis BrusselUpdated: Jul 9, 2026Locations: 1
Eligibility criteria

Adult patients (≥18 years) with severe cancer refractory pain (all types of canc... [+3]

Patients with active, severe infection. [+9]

Status: Recruiting

Intrathecal PD-1/VEGF Bispecific Antibody Plus Pemetrexed for Leptomeningeal Metastasis

Leptomeningeal metastasis, characterized by tumor cells infiltrating and proliferating in the subarachnoid space, represents a distinct pattern of central nervous system involvement and is a fatal complication of malignant tumors. This phase I/II study is to evaluate the recommended dose, safety, feasibility, and therapeutic response of intrathecal PD-1/VEGF bispecific antibody plus pemetrexed in patients with leptomeningeal metastasis.

Participants needed: 34
Trial details
Phase: Phase 1, Phase 2Age: 21-75Biological sex: AllType: InterventionalSponsor: Guangzhou Medical UniversityUpdated: May 20, 2025Locations: 1
Eligibility criteria

Histologically or cytologically confirmed diagnosis of solid tumors;Cerebrospina... [+2]

Any evidence of nervous system failure, including severe encephalopathy, grade 3... [+5]