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A Phase 1/2a Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intrathecally Administered ION717 in Patients with Prion Disease

A Phase 1/2a Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intrathecally Administered ION717 in Patients with Prion Disease

Hingorani Vijay

Ionis Pharmaceuticals, Inc.

2855 Gazelle Court, Carlsbad, CA 92010, USA

vhingorani_contractor@ionis.com

Clinical trial contact

ICON Clinical Research GK

Kyutaromachi 4-chome 1-3, Chuo-ku, Osaka city, Osaka

+81-6-4560-2001

Japan-Chiken@iconplc.com

Not Recruiting

Jan. 31, 2024

Interventional

randomized controlled trial

double blind

placebo control

parallel assignment

treatment purpose

- A confirmed diagnosis of probable or definite prion disease.
- Early-stage prion disease at the time of Screening.
- Willing to meet all study requirements, including travel to Study Center, procedures, measurements and visits.
- Patients must have a caregiver who is >= 18 years old and who is able and willing to facilitate the patient's involvement, to the best of their ability, for the duration of the trial; caregivers must also be able and willing to provide information about themselves and the patient for the duration of the trial.
- Aged >= 18 at the time of informed consent.

- Clinically significant abnormalities in medical history, laboratory tests or physical examination that would render a patient unsuitable for inclusion.
- Any contraindication or unwillingness to undergo an MRI.
- Obstructive hydrocephalus, presence of a functional ventriculoperitoneal shunt for the drainage of cerebrospinal fluid (CSF) or an implanted central nervous system (CNS) catheter.
- Known brain or spinal disease that would interfere with the LP process, CSF circulation or safety assessment.
- Have any other condition, which, in the opinion of the Investigator would make the patient unsuitable for inclusion or could interfere with the patient participating in or completing the study.

Both

prion disease

Regimen 1: ION717 + Placebo
Regimen 2: ION717 + Placebo
Regimen 3: ION717

Incidence of treatment-emergent adverse events (TEAEs) from baseline up to Week 33

- Maximum Observed Plasma Concentration (Cmax) of ION717 on Day 1 and Week 9
- Area Under the Plasma Concentration-time Curve (AUC) of ION717 on Day 1 and Week 9
- Half-life of ION717 in Plasma on Day 1 and Week 9
- Cerebrospinal fluid (CSF) Concentration of ION717 Pre-dose and at multiple points post-dose up to Week 33
- Amount of ION717 Excreted in Urine post-dose on Day 1
- Percent Change from Baseline in Prion Protein (PrP) Concentration in CSF pre-dose and at multiple points post-dose up to Week 33

+81-270-24-3355

Nov. 28, 2023

Yes

Ionis may share anonymized individual participant data, aggregated clinical data, and other types of data that support the results in this study. Data requests from qualified researchers will be considered once all three of the following criteria are met: (1) 12 months from marketing approval of the study drug in both the United States and European Union; (2) 18 months from conclusion of the study; and (3) 6 months from publication of study article. Access would be via a secure environment and is contingent upon approval of a research proposal and entry into an appropriate data use agreement. Requests to access data can be submitted via the website https://vivli.org/ourmember/ionis/.

United States/Canada/Germany/Italy/France/Spain/Israel/Australia