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Clinical Trial Details — Status: Approved for marketing

Administrative data

NCT number NCT04334837
Other study ID # CURCu64Dot0001
Secondary ID
Status Approved for marketing
Phase
First received
Last updated

Study information

Verified date October 2020
Source Curium US LLC
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

This is an open-label, multi-center expanded access program designed to provide access to Copper Cu 64 Dotatate for the detection, localization, and monitoring of NETs to patients that did not have access during the Phase 3 Trial.


Description:

The objective of this trial is to provide patients with confirmed or suspicion of NET access to Copper Cu 64 Dotatate for the detection, localization, and monitoring of SSTR expressing NETs, bridging the gap between investigational product availability in clinical studies and marketed product availability following US Food and Drug Administration (FDA) approval.


Recruitment information / eligibility

Status Approved for marketing
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients of either sex, aged =18 years.

- Willing to sign the Informed Consent Form.

- Able to understand and comply with the procedures and requirements of the program.

- Meet at least one of the following criteria:

1. Confirmed or suspicion of NET based on histology/biopsy report.

2. Confirmed or suspicion of NET based on conventional imaging scans of affected area such as MRI and/or contrast enhanced CT and/or an FDG PET-CT scan and/or NaF PET-CT scan and/or OctreoScan® and/or clinical symptoms performed within 8 weeks prior to administration of Copper Cu 64 Dotatate.

- Negative pregnancy test in women of child-bearing potential, using urine (dip stick test) or blood based testing (within 48 hours of injection).

- For women of childbearing potential, agreement to remain abstinent (refrain from heterosexual intercourse) or use non-hormonal contraceptive methods for at least 2 weeks following administration of investigational product.

- For men, agree to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures for at least 2 weeks following administration of investigational product.

- Recent blood test results (within 4 weeks pre-dose) as follows:

1. WBC: >2 x 109/L

2. Hemoglobin: >8.0g/dL

3. Platelets: >50 x 109/L

4. ALT, AST, AP: =5 times ULN

5. Bilirubin: =3 times ULN

6. Serum creatinine: <170 µmol/L

Exclusion Criteria:

- Pregnant, planning to be pregnant within the next two weeks.

- Therapeutic use of any somatostatin analogue, including Sandostatin® LAR and Lanreotide (within 28 days) and Sandostatin® (within 2 days) prior to administration with Copper Cu 64 Dotatate. If a patient is on Sandostatin® LAR or Lanreotide, a wash-out period of 28 days is required before the injection of the investigational product.

- History or presence of significant hematological abnormalities or immunodeficiency or any condition that might compromise the immune system (infections, vaccinations), of any etiology as indicated by clinically significantly abnormal values of any of the following hematologic parameters: platelets, hemoglobin, WBC count and ANC.

- Lactating and breast-feeding women.

- Acute or chronic clinically significant conditions such as uncontrolled congestive heart failure (rule out with MUGA scan, if suspected), liver or kidney dysfunction, uncontrolled hypertension.

- History of hypersensitivity to drugs with a similar chemical structure to the investigational product or any of its excipients.

- History of significant drug abuse within 1 year prior to administration of Copper Cu 64 Dotatate. Use of soft drugs (such as marijuana) within 3 months prior to the screening visit or hard drugs (such as cocaine, phencyclidine, and crack) within 1 year prior to administration of Copper Cu 64 Dotatate.

- Participation in other clinical research trials involving evaluation of other investigational treatments within 30 days prior to administration of Copper Cu 64 Dotatate and/or unwilling to allow at least one week before participation in another drug trial following administration of Copper Cu 64 Dotatate.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Copper Cu 64 Dotatate
The drug product contains Copper Cu 64 Dotatate filled in a glass vial, closed with butyl rubber stopper secured with an aluminum crimp seal. The drug product will be delivered by Curium to the clinical site. The EAP drug will be administered as an intravenous bolus injection. The dose will be administered according to the schedule detailed in the protocol.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Curium US LLC
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