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NCT Number: NCT06478875

Evaluation of [68Ga]Ga-PentixaFor PET Imaging for the Identification of Unilateral Adrenal Secretion of ALdosterON in Patients With Primary Aldosteronism

PentixaFor radiolabeled with 68Gallium (68Ga) is a radiopharmaceutical targeting the CXC chemokine receptor 4 (CXCR4) receptor. The CXCR4 receptor is expressed in zona glomerulosa of the adrenal cortex and in aldosterone producing adenoma (APA). The objective of this study will be to evaluate in 25 patients if [68Ga]Ga-PentixaFor positron emission tomography ([68Ga]Ga-PTF-PET) imaging allows for the discrimination of patients with lateralized or non-lateralized secretion of aldosterone in adrenal glands classified based on adrenal vein sampling (AVS).

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hôpital européen Georges Pompidou - APHP, Paris, France

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About this study

The identification of the cause of primary aldosteronism (PA) is critical because, in case of lateralized secretion of aldosterone, a surgical treatment can be offered to patients with the objective of full patient recovery, whereas in case of bilateral secretion, only a long-term medical treatment with mineralocorticoid receptor antagonists should be considered. The presence or absence of adrenal nodule on morphological imaging does not allow us to state on the lateralization or not of aldosterone secretion. Moreover, on one hand, the prevalence of adrenal incidentalomas, mostly non-secreting, can be detected in between 2 to 10% of general population. On the other hand, unilateral secretion of aldosterone exists in 30% of patients with normal adrenal glands on imaging. The AVS with measurements of the concentrations of aldosterone is the closest to a referral exam to confirm the diagnosis of lateralized secretion of aldosterone, but it is a complex and invasive procedure with only limited access to centers with expertise in invasive radiology and an important heterogeneity in interpretation. The development of noninvasive imaging approaches allowing for a more specific identification of lateralized vs. bilateral aldosterone secretion would, hence, have a major impact on the clinical management of these patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years old
  • Signed written informed consent
  • French Social Security affiliation
  • For child-bearing aged women, effective form of contraception*
  • Diagnosis of primary aldosteronism:
  • With or without adrenal nodule on morphological imaging (CT or Magnetic Resonance Imaging)
  • With unilateral or bilateral aldosterone secretion confirmed by invasive AVS
  • Such methods include: combined hormonal contraception, progestogen-only hormonal contraception, intrauterine device (IUD) or hormone-releasing system (IUS), bilateral tubal occlusion, vasectomised partner, condom, sexual abstinence.

Exclusion criteria

  • Pregnant or breastfeeding women
  • Patient under legal protection (guardianship)
  • Contraindication to the PET-CT
  • Contraindication to the injection of [68Ga]Ga-PentixaFor
  • Participation in another interventional study involving human participants or being in the exclusion period at the end of a previous study involving human participants, if applicable
  • Patient on AME (state medical aid) (unless exemption from affiliation)
  • Completed group: if the expected number of patients has been reached (15 patients) in the corresponding group of patients (with lateralized or non-lateralized PA).

Treatment and study plan

[68Ga]Ga-PentixaFor PET imaging

Combination Product

PET imaging of adrenal glands

Primary outcomes

  1. relevant biomarkers strongly associated with primary lateralized hyperaldosteronism

    Time frame: 30 days after inclusion

    • Highest max. standardized uptake value (SUVmax) between both adrenal glands on [68Ga]Ga-PTF-PET imaging;
    • Ratio between SUVmax of both adrenal glands on [68Ga]Ga-PTF-PET imaging calculated as highest SUVmax / lowest SUVmax of each adrenal gland;
    • Difference between SUVmax of both adrenal glands on [68Ga]Ga-PTF-PET imaging calculated as the difference highest SUVmax - lowest SUVmax of each adrenal gland;
    • Ratio between the highest SUVmax among both adrenal glands and mean SUV of the liver on [68Ga]Ga-PTF-PET imaging

Secondary outcomes

  1. Aldosterone-to-cortisol ratio between the two adrenal veins on AVS

    Time frame: at inclusion

  2. Lateralization index during AVS

    Time frame: at baseline (during AVS day)

  3. Ratio between the highest SUVmax among both adrenal glands and mean SUV of the liver on [68Ga]Ga-PTF-PET imaging

    Time frame: 30 days after inclusion

  4. Proportion of patients with persistence of PA

    Time frame: 6 months after surgical adrenalectomy

    Patient with a secretion of aldosterone assessed in blood test after surgical adrenalectomy,

  5. CXCR4 expression levels by immuno-histology highest CXCR4 density

    Time frame: 6 months after surgical adrenalectomy

    highest CXCR4 density

  6. Adenoma size on CT

    Time frame: 30 days after inclusion

  7. Adenoma size on histology

    Time frame: 6 months after surgical adrenalectomy

  8. Incidence of Treatment Emergent Adverse Events after [68Ga]Ga-PentixaFor injection (tolerability)

    Time frame: 30 days after [68Ga]Ga-PentixaFor injection

    • Adverse events deemed "medically significant" defined by Allergic and anaphylactic reaction ≥ grade 3 according to CTCAE during or following the injection of the radiopharmaceutical
    • Adverse events of special interest defined by Cutaneous eruption in the three weeks following the injection.
  9. Incidence of Treatment Emergent Serious Adverse Events after [68Ga]Ga-PentixaFor injection (Safety)

    Time frame: 12 months after [68Ga]Ga-PentixaFor injection

    • Serious adverse events (any cause).

Study contacts

Contact information is provided by the study sponsor or research team.

Liliane HAMMANI-BERKANI

CONTACT

[email protected]

0156093762

Touria AL AAMRI

CONTACT

[email protected]

0140271848

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • Pentixapharm AG

Registry information

Official study title

"Pilot Study for the Evaluation of [68Ga]Ga-PentixaFor PET Imaging for the Identification of Unilateral Adrenal Secretion of ALdosterON in Patients With Primary Aldosteronism"

Acronym: PENTALON

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Jun 27, 2024
Registry last updated
Jun 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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