Evaluating the Functional Status of the Adrenal Glands With [68Ga]Ga-PentixaFor in Hyperaldosteronism and Hypercortisolism
Key facts
- Where
- Bethesda, United StatesSee the site
- Phase
- Phase 2
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 120 years old?
Source: NCT06246357, who can take part
Where in United States
- National Institutes of Health Clinical CenterBethesda, United StatesContact: National Cancer Institute Referral OfficeTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- National Cancer Institute (NCI)
- Trial code
- NCT06246357
- Record updated
- 22 October 2026
- Original description
Background:Read full original descriptionShow less
Phase 2 Study Evaluating the Functional Status of the Adrenal Glands With [68Ga]Ga-PentixaFor in Hyperaldosteronism and Hypercortisolism
Background:
The adrenal glands are 2 small organs that sit on top of each kidney. They release hormones; these are chemicals that control how the body works. Tumors on or outside the adrenal glands are called functional if they release hormones; they are called nonfunctional if they do not. Doctors who treat adrenal tumors need to know which type a person has. Researchers want to find better ways to learn whether an adrenal tumor is functional.
Objective:
To see if a new radioactive tracer ([68Ga]Ga-PentixaFor) can make it easier to identify functional adrenal tumors with positron emission tomography (PET) scans.
Eligibility:
People aged 18 years and older with 1 or more adrenal tumors. They must have increased levels of the hormones aldosterone or cortisol. They must also be enrolled in at least 1 other related NIH study (protocols 19-DK-0066, 18-CH-0031, or 09-C-0242).
Design:
Participants will be screened. They may have imaging scans. Their ability to perform normal activities will be reviewed.
Participants will have one PET scan with the study tracer.
The tracer will be given through a tube attached to a needle inserted into a vein. Participants will receive the tracer 1 hour before the scan. They will lie still on a bed while a machine captures images of the inside of their body. The scan will take 45 to 90 minutes.
Participants heart rate, blood pressure, and rate of breathing will be checked before, during, and after the scan.
Participants will have a follow-up visit 3 days after their scan. This visit can be by phone, email, or in person.
Exclusion: Uncontrolled intercurrent illness or social situations based on the review of medical history that would limit compliance with study requirements; Positive beta-human chorionic gonadotropin (beta-HCG) serum or urine pregnancy test performed in females of childbearing potential at screening; Contraindications to having an MRI and CT.
INCLUSION CRITERIA:; Must have any of the following:; one or more adrenal masses on CT and/or MRI and biochemical evidence of excess aldosterone; OR; --ACTH-independent hypercortisolism, with or without adrenal masses on CT and/or MRI; OR; history of ACTH-dependent hypercortisolism (with or without adrenal enlargement); Co-enrollment in 19-DK-0066, 09-C-0242, 18-CH-0031 or a similar NIH trial; Age >=18 years; ECOG performance status <= 2; Women of child-bearing potential (WOCBP) and men must agree to use an effective contraception (barrier, hormonal, intrauterine device [IUD], surgical sterilization, abstinence) for two weeks prior to [68Ga]Ga-PentixaFor scan and for one week after the [68Ga]Ga-PentixaFor scan; Breastfeeding should be discontinued for one week after the [68Ga]Ga-PentixaFor scan; Men must agree not to donate sperm for one week after the [68Ga]Ga-PentixaFor scan; Participants must be able to understand and willing to sign a written informed consent document.