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High-Dose Vitamin C in G6PDA and Pyruvate Kinase Deficiency: A Safety Study (G6PDA PKD)

22 mai 2026 mis à jour par: Jihyun Song, University of Utah

Safety and Tolerability of Supratherapeutic Vitamin C Supplementation in Class A Glucose-6-Phosphate Dehydrogenase (G6PD A) Deficiency and Pyruvate Kinase Deficiency (PKD)

This study is testing whether high-dose Vitamin C is safe and well-tolerated in patients with two inherited red blood cell disorders - Pyruvate Kinase Deficiency (PKD) and Class A Glucose-6-Phosphate Dehydrogenase Deficiency (G6PDA). Both conditions cause red blood cells to break down too quickly, leading to anemia and related complications.

Our earlier research showed that a single oral dose of Vitamin C (250 mg, 500 mg, or 750 mg) reduced red blood cell breakdown by approximately 50% within one hour. This study builds on those findings by testing different doses and frequencies of Vitamin C to find the safest and most effective dosing schedule.

Participants will take Vitamin C once, twice, or three times daily over a 3-week period, with careful monitoring of blood counts, red blood cell survival, iron levels, and any side effects. The study will first enroll 3 adult patients with PKD at Huntsman Cancer Institute. If the results are safe and promising, the study will be extended to patients with G6PDA deficiency, and eventually to children ages 4 and older at Primary Children's Hospital in Salt Lake City.

The goal is to establish a foundation for Vitamin C as a novel therapy to reduce anemia and red blood cell destruction in these rare inherited disorders.

Aperçu de l'étude

Statut

Pas encore de recrutement

Intervention / Traitement

Description détaillée

Pyruvate kinase deficiency (PKD) and Class A Glucose-6-Phosphate Dehydrogenase deficiency (G6PDA) are inherited red blood cell enzyme disorders characterized by chronic hemolytic anemia. Current treatment options are limited and do not fully address the underlying mechanisms of red blood cell destruction, iron overload, and oxidative stress.

Our preliminary studies demonstrated that oral Vitamin C administration at doses of 250 mg, 500 mg, and 750 mg reduced the rate of hemolysis by approximately 50% within one hour of administration, as measured by end-tidal carbon monoxide corrected for ambient CO (ETCOc) - a validated marker of red blood cell breakdown. These findings provide a strong rationale for evaluating the safety and optimal dosing frequency of Vitamin C supplementation in these patient populations.

Study Design:

This is a Phase I, single-site, sequential within-patient dose escalation study. Three adult PKD patients will be enrolled in the initial cohort, each assigned to a different starting dose:

Patient 1: 250 mg daily → 250 mg twice daily → 250 mg three times daily Patient 2: 500 mg daily → 500 mg twice daily → 500 mg three times daily Patient 3: 750 mg daily → 750 mg twice daily → 750 mg twice daily + 500 mg once daily (to reach the NIH-recommended maximum daily dose of 2,000 mg/day)

Each dosing frequency will be maintained for one week, for a total active treatment period of 3 weeks per participant. Safety and hematologic assessments will be performed at baseline and at each dose adjustment visit (9 assessments per participant).

Assessments:

At each visit, participants will undergo:

ETCOc measurement to assess real-time hemolysis Complete blood count and reticulocyte count Metabolic panel including bilirubin and LDH Iron studies including serum iron, transferrin, ferritin, hepcidin, and erythroferrone Vital signs and adverse event assessment

Study Extension:

Following successful completion of the PKD cohort, the study will be extended to G6PDA patients, including 5 G6PDA males and 5 G6PDA heterozygous females from a well-characterized family. A subsequent extension to pediatric patients ages 4 and older is planned at Primary Children's Hospital in Salt Lake City, pending safety and preliminary efficacy data from the adult cohort.

Type d'étude

Interventionnel

Inscription (Estimé)

3

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Lieux d'étude

    • Utah
      • Salt Lake City, Utah, États-Unis, 84112
        • University of Utah
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Confirmed diagnosis of Pyruvate Kinase Deficiency (PKD) or Class A glucose-6-phosphate dehydrogenase (G6PD A) as verified by genetic mutation documentation or enzymatic testing
  • 18 years of age or older
  • Able to take oral medications either by mouth or via gastrostomy tube
  • Willing and able to provide written informed consent prior to any study procedures
  • Heterozygous female carrier of G6PDA deficiency

Exclusion Criteria:

  • Does not have an established diagnosis of Pyruvate Kinase Deficiency (PKD) or Class A Glucose-6-Phosphate Dehydrogenase Deficiency (G6PDA)
  • Unable to tolerate oral medications either by mouth or gastrostomy tube
  • Currently pregnant or planning to become pregnant during the study period
  • Incarcerated individuals
  • Unable to provide written informed consent or assent
  • Known allergy or hypersensitivity to Vitamin C (ascorbic acid)

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation séquentielle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Low Dose Vitamin C (250 mg)
Participants receive oral Vitamin C at 250 mg once daily during Week 1, 250 mg twice daily during Week 2, and 250 mg three times daily during Week 3
Oral pharmacological grade Vitamin C (Ascorbic Acid) administered at escalating doses and frequencies over a 3-week period. Three dose levels are evaluated: 250 mg, 500 mg, and 750 mg, administered once daily (QD), twice daily (BID), or three times daily (TID) depending on the assigned arm. The maximum daily dose does not exceed 2,000 mg/day, consistent with the NIH-recommended maximum daily dose.
Expérimental: Medium Dose Vitamin C (500 mg)
Participants receive oral Vitamin C at 500 mg once daily during Week 1, 500 mg twice daily during Week 2, and 500 mg three times daily during Week 3
Oral pharmacological grade Vitamin C (Ascorbic Acid) administered at escalating doses and frequencies over a 3-week period. Three dose levels are evaluated: 250 mg, 500 mg, and 750 mg, administered once daily (QD), twice daily (BID), or three times daily (TID) depending on the assigned arm. The maximum daily dose does not exceed 2,000 mg/day, consistent with the NIH-recommended maximum daily dose.
Expérimental: High Dose Vitamin C (750 mg)
Participants receive oral Vitamin C at 750 mg once daily during Week 1, 750 mg twice daily during Week 2, and 750 mg twice daily plus 500 mg once daily during Week 3, to reach the NIH-recommended maximum daily dose of 2,000 mg/day
Oral pharmacological grade Vitamin C (Ascorbic Acid) administered at escalating doses and frequencies over a 3-week period. Three dose levels are evaluated: 250 mg, 500 mg, and 750 mg, administered once daily (QD), twice daily (BID), or three times daily (TID) depending on the assigned arm. The maximum daily dose does not exceed 2,000 mg/day, consistent with the NIH-recommended maximum daily dose.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Incidence of Dose-Limiting Toxicities (DLTs)
Délai: From first dose of study intervention through the 28-day safety follow-up visit (approximately 7 weeks per participant)
Number of participants experiencing Grade 3 or higher adverse events as defined by NCI CTCAE v5.0 that are possibly, probably, or definitely related to oral Vitamin C administration at each dose level (250 mg, 500 mg, and 750 mg) and dosing frequency (once daily, twice daily, and three times daily). Hematologic DLTs include Grade ≥3 hemolysis above patient baseline, Grade ≥3 anemia (hemoglobin <8 g/dL), Grade 4 neutropenia (ANC <0.5 × 10⁹/L), and Grade 4 thrombocytopenia (platelet count <25 × 10⁹/L). Non-hematologic DLTs include Grade 3 acute kidney injury, Grade 3 ALT or AST elevation, and any other Grade 3 or higher toxicity considered related to study intervention.
From first dose of study intervention through the 28-day safety follow-up visit (approximately 7 weeks per participant)
Number of Participants With Treatment-Related Adverse Events as Assessed by NCI CTCAE v5.0
Délai: From first dose of study intervention through the 28-day safety follow-up visit (approximately 7 weeks per participant)
Incidence and severity of all adverse events reported during the study, graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE v5.0), including all adverse events possibly, probably, or definitely related to oral Vitamin C administration.
From first dose of study intervention through the 28-day safety follow-up visit (approximately 7 weeks per participant)
Change in Hemoglobin Concentration from Baseline
Délai: Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit
Change in hemoglobin concentration from baseline to each dose adjustment visit, measured by complete blood count (CBC).
Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit
Change in Reticulocyte Count from Baseline
Délai: Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit
Change in reticulocyte count from baseline to each dose adjustment visit, measured by complete blood count (CBC).
Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit
Change in Lactate Dehydrogenase (LDH) from Baseline
Délai: Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit
Change in serum LDH levels from baseline to each dose adjustment visit as a marker of hemolysis.
Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit
Change in Systolic Blood Pressure from Baseline
Délai: Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit
Change in systolic blood pressure from baseline to each study visit as part of vital signs assessment.
Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit
Change in Heart Rate from Baseline
Délai: Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit
Change in heart rate from baseline to each study visit as part of vital signs assessment.
Baseline (Day 1) through Week 3 of treatment and 28-day safety follow-up visit

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

15 juillet 2026

Achèvement primaire (Estimé)

15 juillet 2027

Achèvement de l'étude (Estimé)

15 décembre 2027

Dates d'inscription aux études

Première soumission

19 mai 2026

Première soumission répondant aux critères de contrôle qualité

22 mai 2026

Première publication (Réel)

28 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

28 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

22 mai 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

De-identified individual participant data will be made available upon reasonable request following publication of study results. Data will be stored securely at the Huntsman Cancer Institute and shared in accordance with applicable IRB and institutional data sharing policies.

Délai de partage IPD

Beginning 6 months after primary results publication and available for 5 years thereafter

Critères d'accès au partage IPD

Researchers may submit data access requests to the Principal Investigator (Jihyun Song, PhD) at jihyun.song@utah.edu. Requests will be reviewed on a case-by-case basis.

Type d'informations de prise en charge du partage d'IPD

  • PROTOCOLE D'ÉTUDE
  • SÈVE
  • CIF
  • ANALYTIC_CODE
  • RSE

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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