A Phase 1B Study of IDP-023 g-NK Cells Plus Ocrelizumab in Patients With Refractory Primary and Secondary Progressive Multiple Sclerosis

Indapta Therapeutics, INC.5 个研究点分布在 1 个国家目标入组 34 人开始时间: 2026年6月30日最近更新: 2025年4月30日

适应症

干预措施

试验速览

阶段: 1 期
状态: 暂停
发起方: Indapta Therapeutics, INC.
入组人数: 34
试验地点: 5
主要终点: Incidence of dose-limiting toxicities (DLTs) of IDP-023 in combination with IL-2 and Ocrelizumab (Part 1)

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This is an open label, Phase 1b, multiple ascending dose, and dose-expansion study of IDP-023 administered in combination with interleukin-2 (IL-2) and ocrelizumab to evaluate the safety, tolerability, and biologic activity on autoreactive immune cells in patients with refractory progressive multiple sclerosis.

详细描述

IDP-023 is an off-the-shelf product made from allogeneic g-natural killer (NK) cells, which are a natural subset of NK cells that develop over the course of an immune response in people who have been exposed to the human cytomegalovirus (HCMV). These cells may be particularly effective at targeting and killing the cells that cause the immune system to attack the nervous system in multiple sclerosis (MS). By killing these harmful cells, g-NK cells may help to slow down or potentially stop the progression of MS. When combined with other approved treatments like ocrelizumab, g-NK cells might offer even greater beneﬁt for people with MS.

This is an open label, Phase 1b, multiple ascending dose, and dose-expansion study of IDP- 023 administered in combination with IL-2 and ocrelizumab to evaluate the safety, tolerability, and biologic activity on autoreactive immune cells in patients with primary progressive multiple sclerosis (PPMS) or non-active secondary progressive multiple sclerosis (SPMS).

The study is divided into Part 1, a dose escalation phase, and Part 2, an expansion phase.

Part 1 (Escalation Period): The primary objectives of Part 1 are to deﬁne the safety of different dose levels of IDP-023 in combination with IL-2 and ocrelizumab and to deﬁne the recommended cell dose that will be used for Part 2 (recommended Part 2 dose; RP2D).

Part 2 (Expansion Period): The objective of the Part 2 expansion phase is to assess the biologic activity of IDP-023 in combination with IL-2 and ocrelizumab on autoreactive immune cells in PPMS.

研究设计

研究类型: Interventional
分配方式: Non Randomized
干预模型: Sequential
主要目的: Treatment
盲法: None

入排标准

年龄范围: 18 Years 至 65 Years（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Confirmed diagnosis of primary or non-active secondary progressive MS (SPMS) based on the 2017 revisions of the McDonald criteria.
•Dosed with ocrelizumab within the prior 6 months.
•Expanded Disability Status Scale (EDSS) at screening from 3.0 to 6.5 points.
•Score of ≥2.0 on the Functional Systems (FS) scale for the pyramidal system that is due to lower extremity findings.
•Disease duration from the onset of MS symptoms:
•Less than 15 years in patients with an EDSS at screening >5.
•Less than 10 years in patients with an EDSS at screening ≤5.

排除标准

•Relapsing remitting MS at screening or active SPMS at screening.
•Inability to complete an MRI.
•Contraindication for gadolinium.
•Known presence of other neurological disorders, including but not limited to the following:
•History or known presence of CNS or spinal cord tumor (e.g., meningioma, glioma).
•History or known presence of infectious causes of myelopathy (e.g., syphilis, Lyme disease, Human T-lymphotropic virus 1 [HTLV-1], herpes zoster myelopathy).
•History or known presence of systemic autoimmune disorders potentially causing progressive neurologic disease (e.g., lupus, antiphospholipid antibody syndrome, Sjögren's syndrome, Behçet's disease).
•Impaired cardiac function or history of clinical significant cardiac disease.
•Human immunodeficiency virus (HIV) infection, active hepatitis B infection, or hepatitis C infection.