Condition
Pheochromocytoma clinical trials and research
As of November 12, 2026, Find a Trial lists 22 Pheochromocytoma clinical trials that are recruiting, at sites in 12 countries (most in United States (9), China (3), Argentina (1)). By phase: Phase 2 (4), Phase 1/2 (3), Early Phase 1 (2), Phase 1 (2). There are also 2 NIH-funded research projects on Pheochromocytoma, with $603,936 in listed awards. Every study is explained in plain English. Data from ClinicalTrials.gov and NIH RePORTER, updated November 12, 2026.
- 22Clinical trials
- 2NIH research projects
- 12Countries
Newest Pheochromocytoma clinical trials
All recruiting trials (22)
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Belzutifan and catecholamine metabolism in pheochromocytoma/paraganglioma
This study tests whether Belzutifan can change how catecholamines are produced and broken down in adults with pheochromocytoma or paraganglioma.
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Cardiovascular Outcomes After Adrenalectomy for Pheochromocytoma and Non-secreting Tumors
This study tests how often and what kinds of cardiovascular problems occur after adrenalectomy for pheochromocytoma or non-secreting tumors.
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NET- and somatostatin-targeted PET/SPECT imaging to find and stage neuroblastoma and pheochromocytoma/paraganglioma
This study will try different PET and SPECT tracers to see if they can accurately find and stage tumors in children and adults with neuroblastoma or pheochromocytoma/paraganglioma.
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Evaluating 18F-MFBG PET Imaging for Pheochromocytoma
This study is testing a new imaging method called 18F-MFBG PET to see if it can help people with pheochromocytoma get better and faster pictures of their tumors compared to traditional methods.
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Combining Lutathera® and Olaparib for treating recurrent solid tumors in children and adolescents
This study is testing if combining Lutathera® with olaparib can help children and teenagers with hard-to-treat solid tumors that have certain receptors.
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Registry for Rare Diseases
This study is creating a detailed registry to collect information on rare diseases like amyloidosis and sarcoidosis to help improve how they are diagnosed and treated.
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Understanding genetic causes of neuroendocrine tumors in Mexican patients
This study is trying to find out the genetic changes that cause neuroendocrine tumors in Mexican patients to help develop better treatments.
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Examining the immune system in hereditary pheochromocytoma and paraganglioma
This study is testing how the immune system works in people with pheochromocytoma and paraganglioma, especially those with a family history of these tumors, to see if it can help us find better treatments.
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Targeted treatment for advanced gastrointestinal neuroendocrine tumors and pheochromocytoma
This study is testing a new drug to see if it can help people with advanced gastrointestinal neuroendocrine tumors and pheochromocytoma who have already tried other treatments.
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Advancing genomic medicine using electronic health records
This study is trying to see if using electronic health records and helpful reminders can get more patients tested for genetic conditions in a way that doctors can easily use.
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Treatment for neuroendocrine tumors using 177Lu-DOTATOC
This study is testing a new treatment called 177Lu-DOTATOC to see if it can help patients with certain types of neuroendocrine tumors when other treatments aren't working.
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Omitting preoperative alpha-blockade for normotensive pheochromocytoma
This study is testing whether skipping a common medication before surgery can help patients with certain tumors avoid low blood pressure during and after their operation without putting them at risk.
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Targeted Alpha-Particle Therapy for Advanced SSTR2 Positive Neuroendocrine Tumors
This study is testing a new type of treatment using targeted alpha-particle therapy to see if it can help people with advanced neuroendocrine tumors that have a specific protein called SSTR2.
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Evaluating PARP-1 Expression in Pheochromocytoma and Paraganglioma Using PET/CT Imaging
This study is testing a new imaging method to see how a specific protein is expressed in tumors of patients with pheochromocytoma or paraganglioma before they receive treatment.
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Using 18F-MFBG PET/CT to evaluate neural crest tumors
This study is testing a new imaging method using 18F-MFBG to see if it can help diagnose and better understand tumors like pheochromocytoma, paraganglioma, and neuroblastoma in patients.
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Gene modified immune cells for treating advanced melanoma and metastatic solid tumors
This study is testing if modified immune cells can safely target and attack advanced melanoma and other solid tumors in patients after they receive chemotherapy.
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Evaluation of follow-up care for patients with pheochromocytoma and paraganglioma
This study is testing if a special follow-up care approach can help people with pheochromocytomas and paragangliomas live healthier and longer lives compared to standard care.
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Treatment for inoperable pheochromocytoma and paraganglioma using Lu-177-DOTATATE
This study is testing if a new treatment called Lu-177-DOTATATE can help people with inoperable pheochromocytoma and paraganglioma by delaying the return of their tumors.
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Genetic analysis of tumors related to pheochromocytoma and paraganglioma
This study is trying to find genetic changes in people with pheochromocytomas and paragangliomas to help improve diagnosis and treatment options for them and their families.
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Investigating adrenal tumors and their treatments
This study looks at adrenal tumors and their treatments to see how they develop and what therapies might help patients feel better.
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Using Iodine I 131 Metaiodobenzylguanidine to treat advanced neuroblastoma and pheochromocytoma
This study is testing if a special treatment called Iodine I 131 Metaiodobenzylguanidine can help people with hard-to-treat neuroblastoma and pheochromocytoma feel better when other treatments haven’t worked.
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Improving diagnosis and treatment of pheochromocytoma
This study is testing new ways to find and treat pheochromocytomas, which are tumors from the adrenal glands, to help improve care for people with this condition.
NIH-funded research (2)
Early-stage science funded by the US National Institutes of Health. Most of these projects don't enroll patients, but they show what is being worked on.
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Understanding how genetic background affects rare tumors and their treatment responses
This study is looking at how your genetic background might affect the way rare tumors called pheochromocytomas and paragangliomas behave and respond to treatment, especially for patients from underrepresented racial and ethnic groups, to help find better ways to detect and treat these tumors.
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Understanding genetic factors in hereditary paraganglioma and pheochromocytoma syndrome
This study is looking at how certain genes might affect the chances of developing adrenal tumors called paragangliomas and pheochromocytomas, so if you or someone you know is at risk, this research could help improve testing and treatment options for you.
Related topics
Quick answers
How many Pheochromocytoma clinical trials are recruiting right now?
22, as of November 12, 2026. We update this list each time we refresh our data from ClinicalTrials.gov.
Where are these trials running?
In 12 countries. The most sites are in United States (9 trials), China (3 trials), Argentina (1 trial), South Korea (1 trial), Germany (1 trial). Each study page lists its sites and which ones are recruiting.
What phases are they in?
Phase 2: 4, Phase 1/2: 3, Early Phase 1: 2, Phase 1: 2. Trials with no phase listed are usually device, behavioural or observational studies.
How do I join one?
Open a study, check the "Is this trial a fit for you?" section, then contact the study team listed on the page. They will ask a few screening questions. Asking is free and does not commit you to anything. Talk it over with your doctor first.
Find the studies that fit you
A list is a starting point. Tell us your situation in your own words and we'll rank the studies that match and explain why. It's free and needs no account.