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Baxdrostat and Molecular Imaging of Adrenal Cytoreduction in Primary Aldosteronism (EliXir)

30 agosto 2026 aggiornato da: Queen Mary University of London

Effects of aLdosterone Inhibition by baXdrostat on Molecular Imaging of cytoReduction in Primary Aldosteronism and Hypertension

The goal of this clinical trial is to find out whether treatment with baxdrostat changes aldosterone-producing activity in the adrenal glands of people with primary aldosteronism. The study will use specialised imaging to measure changes in the adrenal glands before and after treatment.

Participants will receive baxdrostat for 24 weeks and will be followed for changes in their adrenal imaging, blood pressure and hormone levels. The study will also investigate whether changes caused by treatment continue after baxdrostat is stopped.

This is a single-group study, meaning that all participants receive baxdrostat and there is no placebo or comparison group.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Primary aldosteronism (PA) is a common cause of hypertension in which the adrenal glands produce excess aldosterone. In some participants, the source of excess aldosterone can be associated with a small adrenal nodule. Aldosterone synthase, encoded by the CYP11B2 gene, is the enzyme responsible for the final steps of aldosterone production.

Molecular imaging using [18F]-CETO PET-CT can be used to visualise aldosterone-producing tissue in the adrenal glands. This study will investigate whether treatment with the aldosterone synthase inhibitor baxdrostat produces a measurable reduction in aldosterone-producing activity on molecular imaging.

This is an open-label, single-arm experimental medicine study. All participants will receive baxdrostat and there is no placebo or control group. Participants will receive baxdrostat 2 mg once daily for 24 weeks. Molecular imaging will be performed before treatment and following the treatment period, allowing the adrenal imaging signal to be compared within the same participant before and after treatment.

The study is designed to investigate whether pharmacological inhibition of aldosterone synthase is associated with a quantitative reduction in the molecular imaging signal from aldosterone-producing adrenal tissue. It will also investigate whether changes in imaging are associated with changes in biochemical measures of aldosterone production and clinical measures such as blood pressure, and how long suppression of aldosterone production persists after treatment has ended.

[18F]-CETO PET-CT is performed following dexamethasone pretreatment to suppress background uptake and improve visualisation of aldosterone-producing adrenal tissue. The radioligand is administered intravenously and PET imaging is performed together with a low-dose anatomical CT scan. Imaging will be undertaken at St Bartholomew's Hospital or Cambridge University Hospitals.

Participants will undergo regular follow-up during and after treatment. Assessments include blood pressure measurements, blood tests for electrolytes and adrenal hormones, 24-hour urine collections for measurement of aldosterone-related biomarkers, and quality-of-life assessment. Follow-up after treatment will allow the investigators to assess whether biochemical and clinical effects of baxdrostat persist after treatment has stopped.

The study also provides an opportunity to investigate the relationship between molecular imaging findings and subsequent clinical management. Where participants subsequently undergo adrenalectomy or ablation as part of their usual clinical care, adrenal tissue may be used for exploratory laboratory analyses of aldosterone synthase expression and markers of apoptosis. Adrenalectomy or ablation is not a research intervention and is not required by the study.

The study uses a within-participant comparison of adrenal molecular imaging before and after baxdrostat treatment. Participants are stratified according to the characteristics of the largest [18F]-CETO-positive adrenal nodule, but there is no randomisation or allocation to different treatment groups.

The study is intended to improve understanding of the effects of aldosterone synthase inhibition on aldosterone-producing adrenal tissue. The findings may help clarify the relationship between biochemical suppression of aldosterone production and changes in adrenal molecular imaging, and may inform the development of future approaches to the treatment and investigation of primary aldosteronism.

Tipo di studio

Interventistico

Iscrizione (Stimato)

30

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion criteria

  • Male or female
  • Age > 18 years at time of signing informed consent.
  • Diagnosed with Primary Aldosteronism (PA) according to Endocrine Society guidelines
  • Presence of one or more adrenal nodules, (diameter 0.5-2.5 cm) on CT, PET-CT, or MRI, with characteristics (e.g. washout) of adenomas
  • Suppressed cortisol after overnight dexamethasone
  • Willing to take baxdrostat for 6 months and attend follow-up visits
  • Willing to undergo PET-CT imaging
  • Estimated glomerular filtration rate ≥ 45 mL/min/1.73m2 at Screening.
  • Serum potassium (K+) level ≥ 3.5 and < 5.0 mmol/L
  • Negative pregnancy test for female participants of childbearing potential
  • Able and willing to provide written consent Exclusion criteria
  • <18 years of age
  • Current or prior treatment (within 1 month before screening) with angiotensin-receptor blockers in combination with ACEIs.
  • Serum sodium level < 135 mmol/L at screening, determined as per central laboratory.
  • The following known secondary causes of hypertension: renal artery stenosis, uncontrolled or untreated hyperthyroidism, uncontrolled or untreated hypothyroidism, pheochromocytoma, Cushing's syndrome, aortic coarctation.
  • New York Heart Association functional Heart Failure class IV at Screening.
  • Known current severe left ventricular outflow obstruction, such as obstructive hypertrophic cardiomyopathy and/or severe aortic valvular disease.
  • Known severe hepatic impairment.
  • Uncontrolled diabetes with HbA1c > 10.0% (86 mmol/mol) at screening.
  • Participants suspected to have severe cardiac hypertrophy.
  • Treatment with any MRAs or potassium-sparing diuretics within 1 month prior to screening.
  • Treatment with potassium binders within 1 month prior to screening.
  • Is expected to receive or is receiving any of the exclusionary drugs such as strong inducers of cytochrome P450 (CYP) 3A, chronic (taken more than 3 times a week for more than 3 months) use of NSAIDs, MRAs or chronic use of systemic steroids.
  • Treatment with K+ supplements is not prohibited but the use should be continuously assessed throughout the trial.
  • Inability or unwillingness to undergo PET-CT imaging
  • Significant comorbidities that would interfere with participation
  • Pregnancy or breastfeeding
  • Unable to give informed consent

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Baxdrostat
Participants will receive baxdrostat 2 mg once daily for 24 weeks. All participants will receive the same intervention; there is no placebo or control group. Participants will undergo study assessments before, during and after treatment, including molecular imaging and biochemical assessments.
Droga: baxdrostat
Baxdrostat 2 mg administered orally once daily for 24 weeks as an aldosterone synthase inhibitor. Treatment begins after the baseline [18F]-CETO PET-CT has confirmed eligibility for study treatment.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in total lesion uptake of [18F]-CETO in adrenal lesions
Lasso di tempo: Baseline to approximately 8 months
Change, between pre- and post-baxdrostat PET-CT images, in total [18F]-CETO-positive lesion uptake, calculated by multiplying the volume (ml) of each lesion by its mean standardised uptake value (SUVmean) (unitless) and summing these values across all lesions. SUVmean is a dimensionless ratio of measured to injected radioactivity. This calculation generates a single reported value, expressed in SUV·ml, the conventional unit for this measurement. [Each lesion will be defined according to the 2025 European Association of Nuclear Medicine guideline.]
Baseline to approximately 8 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in SUVmax between pre- and post-baxdrostat PET-CT images
Lasso di tempo: Baseline to approximately 8 months
Change, between pre- and post-baxdrostat PET-CT images, in maximum standardised uptake value (SUVmax) (unitless) of individual [18F]-CETO-positive lesions. SUVmax is a dimensionless ratio of measured to administered radioactivity. Where more than one lesion is present, SUVmax will be measured separately for each lesion and the values averaged to provide a single participant-level result.
Baseline to approximately 8 months
Voxel level change between pre- and post-baxdrostat PET-CT images
Lasso di tempo: Baseline to approximately 8 months
Voxel-level change in standardised uptake value (SUV) (unitless) between corresponding voxels across [18F]-CETO-positive lesions in pre- and post-baxdrostat PET-CT images. Pre- and post-treatment images will be registered to permit comparison of corresponding voxels, and the mean difference in SUV between paired voxels will be reported. SUV is a dimensionless ratio of measured to injected radioactivity.
Baseline to approximately 8 months
Change in the individual components of the primary endpoint: 1. Volume
Lasso di tempo: Baseline to approximately 8 months
Change, between pre- and post-baxdrostat PET-CT images, in total volume (ml) of all [18F]-CETO-positive lesions. Where more than one lesion is present, individual lesion volumes will be summed to generate a single reported value.
Baseline to approximately 8 months
Change in the individual components of the primary endpoint - 2. mean SUV
Lasso di tempo: Baseline to approximately 8 months
Change, between pre- and post-baxdrostat PET-CT images, in mean standardised uptake value (SUVmean) (unitless) across all [18F]-CETO-positive lesions. Where more than one lesion is present, a single overall SUVmean will be calculated across all lesions. SUVmean is a dimensionless ratio of measured to injected radioactivity.
Baseline to approximately 8 months
Change in whole-adrenal [18F]-CETO uptake
Lasso di tempo: Baseline to approximately 8 months
Change, between pre- and post-baxdrostat PET-CT images, in whole adrenal gland uptake of [18F]-CETO, calculated as the total volume (ml) of adrenal tissue with SUV ≥4 multiplied by the mean standardised uptake value (SUVmean) (unitless) within that volume. This calculation generates a single reported value, expressed in SUV·ml, the conventional unit for this measurement. SUVmean is a dimensionless ratio of measured to injected radioactivity.
Baseline to approximately 8 months
Change in serum aldosterone 12 months after completion of baxdrostat treatment
Lasso di tempo: End of baxdrostat treatment (24 weeks) to 12 months after treatment.
Change, between the end of baxdrostat treatment and 12 months after the end of treatment, in serum aldosterone (pmol/L).
End of baxdrostat treatment (24 weeks) to 12 months after treatment.
Change in plasma renin activity 12 months after completion of baxdrostat treatment
Lasso di tempo: End of baxdrostat treatment (24 weeks) to 12 months after treatment
Change, between the end of baxdrostat treatment and 12 months after the end of treatment, in plasma renin activity (nmol/L/hr).
End of baxdrostat treatment (24 weeks) to 12 months after treatment
Change in 24-hour urinary tetrahydroaldosterone 12 months after completion of baxdrostat treatment
Lasso di tempo: End of baxdrostat treatment (24 weeks) to 12 months after treatment
Change, between the end of baxdrostat treatment and 12 months after the end of treatment, in 24h urine tetrahydroaldosterone (micromoles per 24h).
End of baxdrostat treatment (24 weeks) to 12 months after treatment
Change in systolic blood pressure 12 months after completion of baxdrostat treatment
Lasso di tempo: End of baxdrostat treatment (24 weeks) to 12 months after treatment
Change, between the end of baxdrostat treatment (24 weeks) and 12 months after the end of treatment, in systolic blood pressure (mmHg).
End of baxdrostat treatment (24 weeks) to 12 months after treatment
Change in aldosterone-to-renin ratio 12 months after completion of baxdrostat treatment
Lasso di tempo: End of baxdrostat treatment (24 weeks) to 12 months after treatment
Change, between the end of baxdrostat treatment (24 weeks) and 12 months after the end of treatment, in the ratio of serum aldosterone (pmol/L) to plasma renin activity (nmol/L/hr). The single measure resulting from division of aldosterone by plasma renin activity, termed the aldosterone-to-renin ratio (ARR), is expressed in (pmol/L)/(nmol/L/hr).
End of baxdrostat treatment (24 weeks) to 12 months after treatment
Change in serum 11-deoxycorticosterone after 12 weeks of baxdrostat treatment
Lasso di tempo: Baseline to 12 weeks
Change, between baseline and 12 weeks of baxdrostat treatment, in serum 11-deoxycorticosterone (11-DOC) (pmol/L).
Baseline to 12 weeks
Change in serum 11-deoxycorticosterone after 24 weeks of baxdrostat treatment
Lasso di tempo: Baseline to 24 weeks
Change, between baseline and 24 weeks of baxdrostat treatment, in serum 11-deoxycorticosterone (11-DOC) (pmol/L).
Baseline to 24 weeks
Change in serum 11-deoxycorticosterone 2 months after completion of baxdrostat treatment
Lasso di tempo: Baseline to 2 months after completion of baxdrostat treatment
Change, between baseline and 2 months after completion of baxdrostat treatment, in serum 11-deoxycorticosterone (11-DOC) (pmol/L).
Baseline to 2 months after completion of baxdrostat treatment
Change in serum 11-deoxycorticosterone 6 months after completion of baxdrostat treatment
Lasso di tempo: Baseline to 6 months after completion of baxdrostat treatment
Change, between baseline and 6 months after completion of baxdrostat treatment, in serum 11-deoxycorticosterone (11-DOC) (pmol/L).
Baseline to 6 months after completion of baxdrostat treatment
Change in serum 11-deoxycorticosterone 12 months after completion of baxdrostat treatment
Lasso di tempo: Baseline to 12 months after completion of baxdrostat treatment
Change, between baseline and 12 months after completion of baxdrostat treatment, in serum 11-deoxycorticosterone (11-DOC) (pmol/L).
Baseline to 12 months after completion of baxdrostat treatment

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Queen Mary University of London

Collaboratori

AstraZeneca

Investigatori

  • Investigatore principale: Morris J Brown, FMedSci, FRS, Queen Mary University of London

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

15 settembre 2026

Completamento primario (Stimato)

31 maggio 2028

Completamento dello studio (Stimato)

31 maggio 2028

Date di iscrizione allo studio

Primo inviato

20 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

30 agosto 2026

Primo Inserito (Effettivo)

2 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

2 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

30 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • 371884

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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