Tralement Versus a Fixed-dose Trace Element Combination Product to Evaluate Manganese Safety

American Regent

Status and phase: Withdrawn; Phase 4

Conditions: Manganese Safety in Adults

Treatments: Drug: Fixed-dose trace element combination product of zinc, copper, and selenious acid; Drug: Tralement

Study type: Interventional

Funder types: Industry

Identifiers

NCT05661682

TE20001

Details and patient eligibility

About

Tralement versus a fixed-dose trace element combination product of zinc, copper, and selenious acid to evaluate product safety in adult patients requiring long-term parenteral nutrition.

Full description

A Phase IV, multi-center, randomized single-blind trial to evaluate the safety profile of Tralement versus a fixed-dose trace element product of zinc, copper, and selenious acid in adult patients who are expected to require at least six-months of home parenteral nutrition.

This study will enroll new prescribed home parenteral nutrition users, i.e. a patient enrolled in the study within six weeks of initiating first-time use of parenteral nutrition requiring trace element additives. Note: a portion of patients who meet inclusion criteria may have received parenteral nutrition in an inpatient setting before discharge home.

Eligible participants who satisfy the inclusion requirements and no exclusion criteria will be consented to participate in this study and enter the screening study phase.

The screening evaluation will be conducted within 5 days of the dose administration of study drug. Study participants meeting entry criteria of normal brain MRI and laboratory manganese concentrations (whole blood/plasma/serum/RBC) will begin study drug on Day 1.

Participants will undergo 2 additional post-baseline brain MRI scans at Months 3 and 6 and have 5 separate neuropsychological tests at Day 1, Month 3, and Month 6. Additional clinical monitoring including safety and laboratory assessments will occur during the 6-month opt-in extension study.

All patients in each assigned trace element parenteral nutrition group will have parenteral nutrition formulations evaluated for manganese content at Day 1, Month 1, Month 3, and Month 6.

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult (≥18 to ≤80 years of age) participants able to provide informed consent.
• Male and female participants who are new users to home parenteral nutrition as a source of trace elements when oral or enteral nutrition is not possible, insufficient, or, contraindicated.
• Anticipated duration of home parenteral nutrition use is 6 months or greater.
• A normal baseline brain MRI scan.
• A normal blood manganese concentration.
• Ability to undergo additional 2 brain MRI scans over the six-month study period (Sedation, if appropriate, to be determined by the Principal Investigator's study site, institutional review board recommendations).
• Definitive contraception for females of reproductive age.

Exclusion criteria

• Prior parenteral nutrition therapy.
• Hypersensitivity or allergy to zinc or copper.
• History of occupational exposure to manganese and documented by laboratory test results.
• Baseline ferritin ≥300 ng/mL or below 100 ng/mL.
• Baseline transferrin saturation (TSAT) ≥45 % or below 20%.
• Prior or current cholestatic liver disease defined as a clinical condition associated with decrease in bile flow due to impaired secretion by hepatocytes or to obstruction of bile flow through intra-or extrahepatic bile ducts.
• Liver function studies with transaminases greater than two-fold normal or total bilirubin >2 mg/dL.
• Brain MRI exclusion criteria: MRI-unsafe metal implants, claustrophobia.
• Known excess environmental exposure to manganese.
• Less than 1-year expected survival, as anticipated by their primary provider.
• Current participation in another clinical trial.
• Females in pregnant state.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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0 participants in 2 patient groups

Tralement

Active Comparator group

Description:

This study will enroll new prescribed home parenteral nutrition users, i.e. a patient enrolled in the study within six weeks of initiating first-time use of parenteral nutrition formulation requiring trace element additives. Note: a portion of patients who meet inclusion criteria may have received parenteral nutrition in an inpatient setting before discharge home.

Treatment:

Drug: Tralement

a fixed-dose trace element combination product of zinc sulfate, copper sulfate, and selenious acid

Active Comparator group

Description:

This study will enroll new prescribed home parenteral nutrition users, i.e. a patient enrolled in the study within six weeks of initiating first-time use of parenteral nutrition formulation requiring trace element additives. Note: a portion of patients who meet inclusion criteria may have received parenteral nutrition in an inpatient setting before discharge home.

Treatment:

Drug: Fixed-dose trace element combination product of zinc, copper, and selenious acid