A Phase 2 interventional study of BR55 in Ovarian Cancer, sponsored by Bracco Diagnostics, Inc. Terminated at 1 site in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-08-23.
Sponsored by Bracco Diagnostics, Inc (part of Bracco) · Phase 2, Interventional, and Diagnostic
This is an exploratory, single center, open label, prospective study of BR55 to determine the optimal phase of the menstrual cycle for performing BR55 contrast-enhanced ultrasonography (CEUS) of the target ovary in premenopausal women scheduled to undergo preventative surgery because of high familial/hereditary or genetic risk for ovarian cancer.
2,757 studies on the registry are indexed under Ovarian Neoplasms; 735 are open to participants now.
This study's enrollment of 3 is below the median of 59 across 2,075 interventional studies indexed under Ovarian Neoplasms.
Browse Ovarian Neoplasms studies →Bracco Diagnostics, Inc is the lead sponsor of 49 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Inclusion Criteria: Enroll a subject in this study if the subject meets the following inclusion criteria:
Exclusion Criteria: Exclude a subject from this study if the subject does not fulfill the inclusion criteria, or if any of the following conditions are observed:
Is a pregnant or lactating female. Exclude the possibility of pregnancy:
BR55 will be performed in the early follicular phase first and in the late follicular phase thereafter.
Drug: BR55
BR55 will be performed in the late follicular phase first and in the early follicular phase thereafter.
Drug: BR55
BR55 will be administered at doses of 0.03 mL/kg or 0.05 mL/kg
Adverse Events
Number of participants who received the contrast agent and experienced an adverse event.
Time frame: From the time of signing Informed Consent through 24 hours post-dose, up to a maximum of 11 days
| Milestone | Training Cases | Group A | Group B |
|---|---|---|---|
| Started | 3 | 0 | 0 |
| Completed | 3 | 0 | 0 |
| Not completed | 0 | 0 | 0 |
Number of participants who received the contrast agent and experienced an adverse event.
| Participants | Training Cases | Group A | Group B |
|---|---|---|---|
| Adverse Events | 0 | — | — |
Collected over Safety monitoring was to begin at the time of signing Informed Consent through 24 hours post-dose, up to a maximum of 11 days.. Non-serious events are listed at a 5% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Training Cases | 0/3 (0%) | 0/3 (0%) | 0/3 (0%) |
| Group A | — | — | — |
| Group B | — | — | — |
The only participants enrolled in this study were 3 "training cases." No other study participant was enrolled in the study; therefore, there are no results for Group A and Group B.
| Age, Categorical(Participants) | Training Cases | Group A | Group B | Total |
|---|---|---|---|---|
| <=18 years | 0 | — | — | 0 |
| Between 18 and 65 years | 3 | — | — | 3 |
| >=65 years | 0 | — | — | 0 |
| Age, Continuous(years) | Training Cases | Group A | Group B | Total |
|---|---|---|---|---|
| Mean | 38.3 (35 to 43) | — | — | 38.3 (35 to 43) |
| Sex: Female, Male(Participants) | Training Cases | Group A | Group B | Total |
|---|---|---|---|---|
| Female | 3 | — | — | 3 |
| Male | 0 | — | — | 0 |
| Race (NIH/OMB)(Participants) | Training Cases | Group A | Group B | Total |
|---|---|---|---|---|
| American Indian or Alaska Native | 0 | — | — | 0 |
| Asian | 0 | — | — | 0 |
| Native Hawaiian or Other Pacific Islander | 0 | — | — | 0 |
| Black or African American | 0 | — | — | 0 |
| White | 3 | — | — | 3 |
| More than one race | 0 | — | — | 0 |
| Unknown or Not Reported | 0 | — | — | 0 |
| Region of Enrollment(participants) | Training Cases | Group A | Group B | Total |
|---|---|---|---|---|
| United States | 3 | — | — | 3 |
| Actual Volume (mL) Injected(mL) | Training Cases | Group A | Group B | Total |
|---|---|---|---|---|
| Mean | 2.06 (1.86 to 2.41) | — | — | 2.06 (1.86 to 2.41) |
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Plan to share: No
This study is terminated, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: BR55