Define the Optimal Uptake Time of 68Ga-OPS202 When Used as a PET (Positron Emission Tomography) Imaging Agent in Subjects With Newly Diagnosed Breast Cancer

Breast Cancer Clinical Trial

Official title:

A Non-Randomised Phase II Study to Evaluate the Optimal Uptake Time of 68GA-OPS202 as a sstr2 Positive PET Imaging Agent in Subjects With Newly Diagnosed Breast Cancer

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03697551
• Other study ID #: D-FR-01070-003
• Secondary ID: 2018-000028-33
• Status: Terminated
• Phase: Phase 2
• Start date: October 22, 2018
• Est. completion date: February 6, 2019

Study information

• Verified date: August 2020
• Source: Ipsen
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this clinical research is to define the optimal uptake time of 68Ga-OPS202 as a PET imaging agent to be used to detect and localize breast cancer somatostatin receptor subtype 2 (SSTR2) positive lesions.

68Ga-OPS202 is a radiolabelled imaging agent to be used in association with PET. 68Ga-OPS202 is made of two main components: 1) OPS202, an antagonistic somatostatin analogue which binds to the somatostatin receptor (type 2) present on the surface of the tumor cells and 2) Gallium 68, a radioisotope that, combined with OPS202, can be seen in the PET scanner.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 4
• Est. completion date: February 6, 2019
• Est. primary completion date: February 6, 2019
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Women aged 18 years or older

• Subjects with newly diagnosed (early or advanced) breast cancer

• Eastern Cooperative Oncology Group (ECOG) performance status =2

• Adequate bone marrow, liver and renal function, with:

• Calculated glomerular filtration rate (GFR): =45 mL/min

• Albumin: >30 g/L

• Alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (AP): =5 times upper limit of normal (ULN)

• Bilirubin: =3xULN (3×1.1 mg/dL)

• Leukocytes: =3x109/L, and neutrophils: =1x109/L

• Erythrocytes: =3.5x1012/L

• Platelets: =90x109/L

• Signed written informed consent prior to any study-related procedures.

Exclusion Criteria:

• Subject with resected primary tumour

• Subjects with confirmed ductal carcinoma in situ

• Men with breast cancer

• Presence of an active infection at screening or history of a serious infection within the previous 6 weeks prior to the first 68Ga-OPS202 administration that might interfere with the PET and/or CT analysis

• Subjects who have received any therapy for breast cancer

• Prior or planned administration of a radiopharmaceutical within 8 half-lives of the radionuclide

• Clinically relevant trauma within 2 weeks prior to first 68Ga-OPS202 administration

• Any condition that precludes the proper performance of PET and/or CT scan:

• Subjects who are not able to tolerate the CT contrast agent

• Subjects with metal implants or arthroplasty, or any other objects that might interfere with the PET and/or CT analysis

• Subjects unable to raise arms for prolonged imaging purposes

• Subjects unable to lie still for the entire imaging time

• Subjects weighing greater than 110 kg (243 lb)

• Known hypersensitivity to radiolabelled NODAGA (1,4,7- triazacyclononane,1-glutaric acid 4,7 acetic acid), to Gallium-68, to somatostatin analogue peptide JR11 or to any of the excipients of 68Ga- OPS202

• History of, or current active allergic or autoimmune disease, including asthma or any condition requiring long-term use of systemic corticosteroids

• Known human immunodeficiency virus (HIV) or positive serology for HIV, hepatitis B or C

• Administration of another investigational medicinal product within 30 days prior to first 68Ga-OPS202 administration

• Subjects who are pregnant, breast feeding or of childbearing potential not willing to practice effective contraceptive techniques during the study treatment period and for 30 days after the last dose of 68Ga-OPS202 administration; pregnancy test must be performed at the start of the study and prior to 68Ga-OPS202 administration

• Subjects who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study, including any mental condition rendering the subject unable to understand the nature, scope, and possible consequences of the study, and/or evidence of an uncooperative attitude

• Subject who experienced a previous cancer (except basocellular carcinoma of the skin and/or in situ carcinoma of the cervix/uterus), and/or subjects treated with curative intent and free from disease for more than 5 years

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• Satoreotide trizoxetan
Subjects will receive a single dose of Satoreotide trizoxetan consisting of a peptide mass up to 45 µg, with a radioactivity range of 150-200 MBq. Satoreotide trizoxetan is intended for diagnostic use as a Positron emission tomography/computed tomography (PET/CT) tracer for the imaging of tumours expressing SSTR2.

Locations

Country	Name	City	State
Austria	Medical University Innsbruck	Innsbruck

Sponsors (1)

Lead Sponsor	Collaborator
Ipsen

Country where clinical trial is conducted

Austria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of Subjects With Sufficiently Avid Lesion(s) Identified as a sstr2 Positive Lesion (Co-Primary Endpoint)	The percentage of subjects with sufficiently avid lesion(s) to be identified as a sstr2 positive lesion using 68Ga-satoreotide trizoxetan was to be determined.	At 0.5, 1.0 and 2.0 hours post injection on Day 1.
Primary	Differences in the Number of Lesions Detected by 68Ga-Satoreotide Trizoxetan Between the 3 PET Acquisition Timepoints in Primary Breast Lesions (Co-Primary Endpoint)	The differences in the number of lesions detected by 68Ga-satoreotide trizoxetan between the 3 PET acquisition timepoints, and reader interpretation was to be determined.	0.5, 1.0 and 2.0 hours post injection on Day 1