Intraventricular Administration of Rhenium-186 NanoLiposome for Leptomeningeal Metastases

Leptomeningeal Metastasis Clinical Trial

— ReSPECT-LM  

Official title:

A Multicenter Phase 1 Clinical Study to Determine the Maximum Tolerated Dose/Maximum Feasible Dose, Safety,& Efficacy of Single Dose Rhenium-186 NanoLiposome (186RNL) Administered Via Intraventricular Catheter for Leptomeningeal Metastases

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05034497
• Other study ID #: 2021-LM-001
• Status: Recruiting
• Phase: Phase 1
• Start date: December 6, 2021
• Est. completion date: June 30, 2026

Study information

• Verified date: May 2024
• Source: Plus Therapeutics
• Contact: Melissa Moore, PhD
• Phone: 1-347-570-3338
• Email: MMoore[@]plustherapeutics.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is an open-label Phase I clinical study that will administer a single dose of 186RNL via intraventricular catheter for treatment of Leptomeningeal Metastases (LM).

Description:

This Phase I clinical study evaluates a single dose of 186RNL (radionuclide clinical study drug) administered through an intraventricular catheter (Ommaya reservoir) in participants with Leptomeningeal Metastases (LM). The clinical study treatment consists of a single administered 5cc dose of 186RNL per participant. The clinical study will include the evaluation at separate dose levels. Three to six participants may be treated at each dose. The maximum number of participants to be enrolled in the study is 27. The clinical study treatment will be administered, following a CSF flow study, on an outpatient basis by the clinical study physician. Participants will be followed for up to 12 months after the clinical study drug is administered. The U.S. Food and Drug Administration (FDA) has not approved 186RNL for this specific disease.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 18
• Est. completion date: June 30, 2026
• Est. primary completion date: December 21, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. At least 18 years of age at time of screening.

2. Ability to understand the purposes and risks of the study and has signed a written informed consent document approved by the site-specific IRB.

3. Subject has proven and documented LM that meets the requirements for the study:

a. Current EANO-ESMO Clinical Practice Guidelines Type 1 and 2 LM of any primary type. 2D is excluded.

4. Karnofsky performance status of 60 to 100.

5. Acceptable liver function:

• Bilirubin 1.5 times upper limit of normal
• AST (SGOT) and ALT (SGPT) = 3.0 times upper limit of normal for subjects with normal liver
• AST (SGOT) and ALT (SGPT) = 5.0 times upper limit of normal for subjects with liver metastasis
• Acceptable renal function with serum creatinine = 2 times upper limit of normal

6. Acceptable hematologic status (without hematologic support):

• ANC = 1000 cells µL
• Platelet count = 75,000/µL
• Hemoglobin = 9.0 g/dL

7. All women of childbearing potential must have a negative serum pregnancy test at screening. Male and female subjects must agree to use effective means of contraception (for example, surgical sterilization or the use of barrier contraception with either a condom or diaphragm in conjunction with spermicidal gel or an IUD) with their partner from entry into the study through 6 months after the last dose.

8. Subjects with a creatinine clearance greater than or equal to 60 mL/min (using the Cockcroft-Gault Equation) for males and females.

Exclusion Criteria:

1. The subject has not recovered to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE v5.0) Grade = 1 from AEs due to antineoplastic agents, investigational drugs, or other medications that were administered prior to study. Prior AEs due to alopecia, anemia, and lymphopenia are not required to be recovered to Grade = 1 prior to 186RNL treatment, assuming other inclusion criteria are satisfied.

2. Obstructive or symptomatic communicating hydrocephalus.

3. Ventriculo-peritoneal or ventriculo-atrial shunts without programable valves or contraindications to placement of Ommaya reservoir.

4. Females of childbearing potential who are pregnant, breast feeding, or may possibly be pregnant without a negative serum pregnancy test (see inclusion criteria).

5. Serious intercurrent illness, such as progressive systemic (extra leptomeningeal) disease, clinically significant cardiac arrhythmias, uncontrolled systemic infection, symptomatic congestive heart failure or unstable angina pectoris within 3 months prior study drug, myocardial infarction, stroke, transient ischemic attack within 6 months, seizure disorder with any seizure occurring within 14 days prior to consenting or encephalopathy.

6. Active severe non hematologic organ toxicity such as renal, cardiac, hepatic, pulmonary, or gastrointestinal systemic toxicity grade 3 or above.

7. Significant coagulation abnormalities such as inherited bleeding diathesis or acquired coagulopathy with unacceptable risks of bleeding.

8. Patients who had any dose to the spinal cord or whole brain radiation therapy, regardless of when the radiation treatment was delivered. Prior, non-CNS radiation for primary tumor is allowed.

9. Systemic chemotherapeutic agents with CNS penetration (such as temozolomide, carmustine, lomustine, capecitabine, carboplatin, vinorelbine, bevacizumab, irinotecan or topotecan) are excluded if given within 14 days or 5 half-lives, whichever is shorter, prior to 186RNL treatment.

1. If the washout period is satisfied, the patient may be enrolled, providing all other I/E criteria are satisfied.

2. If the patient is undergoing systemic chemotherapy with CNS penetration (such as temozolomide, carmustine, lomustine, capecitabine, carboplatin, vinorelbine, bevacizumab, irinotecan or topotecan) and they develop or have progressive/persistent LM while on the agent, they may be included in the trial at the PI's discretion.

10. Systemic therapy (including investigational agents and small-molecule kinase inhibitors) is excluded if given within 14 days or 5 half-lives, whichever is shorter, prior to 186RNL treatment. a. If the washout period is satisfied, the patient may be enrolled, providing all other I/E criteria are satisfied.

11. Nitrosoureas or mitomycin C within 42 days, or metronomic/protracted low-dose chemotherapy within 14 days, or other cytotoxic chemotherapy within 28 days, are excluded if given within the above timepoints prior to 186RNL treatment. a. If the washout period is satisfied, the patient may be enrolled, providing all other I/E criteria are satisfied.

12. Impaired CSF Flow Study, within 4 +/- 3 days of 186RNL treatment, based on study imaging and as determined by the investigator.

Related Conditions & MeSH terms

• Leptomeningeal Metastasis
• Meningeal Carcinomatosis
• Neoplasm Metastasis

Intervention

Drug:
• 186RNL
All participants will be required to have an Ommaya Reservoir and a CSF Flow Study. Participants will receive a single 5cc dose of 186RNL via Ommaya Reservoir.

Locations

Country	Name	City	State
United States	Northwestern Memorial Hospital Olson Pavilion	Chicago	Illinois
United States	Ohio State University Hospital	Columbus	Ohio
United States	Universiy of Texas Southwestern Medical Center	Dallas	Texas
United States	The University of Texas MD Anderson Cancer Center	Houston	Texas
United States	UT Health Science Center San Antonio / Mays Cancer Center	San Antonio	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Plus Therapeutics

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence and severity of adverse events (AE) and serious adverse events (SAE)	Safety will be evaluated by the incidence of AEs and SAEs graded according CTCAE version 5.0.	12 months
Primary	Incidence of dose-limiting toxicities (DLT)	Maximum Tolerated Dose (MTD) will be evaluated by testing increasing doses with 3 to 6 participants in each cohort. MTD reflects the highest dose of drug that did not cause a Dose-Limiting Toxicity (DLT) in > 33% of participants.	12 months
Secondary	Determination of the overall response rate (ORR)	Determine the overall response rate (ORR) defined as the proportion of all evaluable participants achieving a response as the best overall response at the time of progression.	12 months
Secondary	Determination of the duration of response (DoR)	Determine the duration of response (DoR) defined as the time from first response to LM progression.	12 months
Secondary	Determination of progression free survival (PFS)	Determine progression free survival (PFS) defined as the time from first treatment to date of LM progression or death from any cause.	12 months
Secondary	Overall survival (OS)	Determine the overall survival (OS) define as the time from first treatment to date of death.	12 Months