Combining Active and Passive DNA Hypomethylation: A Randomized, Placebo-Controlled Phase II Study of the Efficacy and Safety of Oral Vitamin C in Combination With Azacitidine in Patients With Higher-Risk MDS, CMML-2 or Low-Blast Count AML

Who is this study for? Patients with Myelodysplastic Syndromes, Acute Myeloid Leukemia
What treatments are being studied? Vitamin C
Status: Recruiting
Location: See all (10) locations...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is a multicentre, randomized, parallel-group, placebo-controlled, double-blind phase 2 study of the efficacy and safety of oral vitamin C supplement in combination with azacitidine in patients with higher-risk MDS, CMML-2 or low-blast count AML. The primary purpose is to investigate if oral vitamin C supplementation to azacitidine, compared with azacitidine + placebo, can increase the effectiveness of epigenetic therapy in patients with higher-risk myeloid malignancies, who are not candidates for allogeneic hematopoietic stem cell transplantation.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ • Patients eligible for treatment with azacitidine with one of the following diagnoses according to World Health Organization 2016:

• MDS Higher-risk MDS according to the IPSS-R, i.e., intermediate- to very high-risk (IPSS-R score \> 3)

• CMML CMML with 10-29 percent marrow blasts without myeloproliferative disorder

• AML AML with 20-30 percent blasts (low-blast count AML)

⁃ Note: Patients with therapy-related MDS are eligible if they have not received radiation or chemotherapy for six months.

Locations
Other Locations
Denmark
Aalborg University Hospital
RECRUITING
Aalborg
Aarhus University Hospital
RECRUITING
Aarhus
Herlev University Hospital
RECRUITING
Copenhagen
Rigshospitalet
RECRUITING
Copenhagen
Odense University Hospital
ACTIVE_NOT_RECRUITING
Odense
Zealand University Hospital
TERMINATED
Roskilde
Sweden
Sahlgrenska University Hospital
RECRUITING
Gothenburg
Skåne University Hospital
RECRUITING
Lund
Karolinska University Hospital
RECRUITING
Stockholm
Uppsala University Hospital
RECRUITING
Uppsala
Contact Information
Primary
Kirsten Grønbæk, Prof., MD
kirsten.groenbaek@regionh.dk
+45 35 45 60 86
Backup
Krista Smidt Bech, BSc, Nurse
krista.smidt.bech.01@regionh.dk
+45 35 45 60 80
Time Frame
Start Date: 2019-09-11
Estimated Completion Date: 2027-12
Participants
Target number of participants: 196
Treatments
Experimental: Vitamin C
Oral vitamin C (ascorbic acid) will be given in a dose of 1000 mg daily (two capsules of 500 mg once daily) starting day 1 in the 1st azacitidine (AZA) cycle (D1/C1) and continuing until discontinuation of AZA or end of study, whichever occurs earlier.
Placebo_comparator: Placebo
Placebo will be administered orally as two capsules once daily that look and taste identical to the capsules containing vitamin C. Treatment will start day 1 in the 1st azacitidine (AZA) cycle (D1/C1) and continuing until discontinuation of AZA or end of study, whichever occurs earlier. The content of the placebo capsules is glucose monohydrate, potato starch, gelatin, magnesium stearate and talc.
Authors
Amalie Bach Nielsen, Stine Ulrik Mikkelsen
Sponsors
Leads: Kirsten Grønbæk
Collaborators: University of Southern California, Karolinska University Hospital, Van Andel Institute - Stand Up To Cancer Epigenetics Dream Team, Zealand University Hospital, Odense University Hospital, Uppsala University Hospital, Skane University Hospital, Aarhus University Hospital, University of Copenhagen, Imperial College London, Technical University of Denmark, Aalborg University Hospital, Sahlgrenska University Hospital

This content was sourced from clinicaltrials.gov

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