Bioequivalence of Azacitidine 300 mg Film-Coated Tablets in Adult Patients With Acute Myeloid Leukaemia (AML)

NCT06326697 | Completed Phase 1

• 1 other identifier: HIK-AZA-2023-01
• Study Type: interventional
• Target: 32
• Locations: 1 country
• Sites: 1

Brief Summary

A Randomized, Single Oral Dose, Open Label, Two Treatment, Crossover study to investigate the bioequivalence of the Test Product Azacitidine 300 mg Film coated tablets relative to Reference Product Onureg® 300 mg Film Coated Tablets in adult patients with AML under fasting conditions

Conditions

Acute Myeloid Leukaemia

Outcome Measures

Primary Outcomes (2)

• Cmax

  Maximum measured plasma concentration over the time span specified

  5 hours

• AUC0-t

  The area under the plasma concentration versus time curve, from time (0) to the last measurable concentration (t), as calculated by the linear trapezoidal method.

  5 hours

Secondary Outcomes (6)

• AUC0-∞

  5 hours

• Kel

  5 hours

• Tmax

  5 hours

• T1/2el

  5 hours

• Adverse Events (AEs)

  Day 4

Study Arms (2)

Test Product: Azacitidine 300 mg Film coated tablets

EXPERIMENTAL

Single oral dose of Azacitidine 300 mg Film coated tablets

Drug: Azacitidine

Reference Product: Onureg® 300 mg Film Coated Tablets

ACTIVE COMPARATOR

Single oral dose of Onureg® 300 mg Film Coated Tablets

Drug: Onureg

Interventions

Azacitidine DRUG

Azacitidine 300 mg Film coated tablets

Test Product: Azacitidine 300 mg Film coated tablets

Onureg DRUG

Azacitidine 300 mg Film coated tablets

Reference Product: Onureg® 300 mg Film Coated Tablets

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients age ≥ 18 years of age at the time of signing the informed consent document.
• Patients with documented diagnosis of AML according to the 2022 updates of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukaemia.
• Patients with acute myeloid leukemia who achieved first complete remission or complete remission with incomplete blood count recovery following intensive induction chemotherapy and are not able to complete intensive curative therapy. The definitions of response criteria for CR or CRi are primarily those defined by the 2022 report from the European Leukemia Net (ELN) on AML as below: CR defined as bone marrow blasts \<5%; absence of circulating blasts; absence of extramedullary disease; ANC ≥ 1.0 × 10\^9/L (1,000/µL); platelet count ≥ 100 × 10\^9/L(100 000/µL).
• CRi defined as all CR criteria, except for residual neutropenia \< 1.0 × 10\^9/L (1,000/µL) or thrombocytopenia \< 100 × 10\^9/L (100 000/µL).
• Patients who don't have a known or suspected hypersensitivity to Azacitidine or any other ingredient used in the manufacturing of Azacitidine.
• Patients who are physically able for appropriate pharmacokinetics sampling according to principal investigator evaluation.
• Patients who have a haematological profile appropriate for receiving Azacitidine 300 mg dose for 4 consecutive days as per the principal investigator assessment.
• Patients who understand and voluntarily sign a written informed consent document prior to any study related assessments/procedures are conducted.
• Patient is capable of consent.
• Females of childbearing potential may participate, providing the subject meets the following conditions: Negative serum pregnancy test at screening (sensitivity of at least 25 mIU/mL), and willing to use effective contraception during and up to 6 months after study.
• Male patients must be willing to use effective contraception during and up to 3 months after the study.

You may not qualify if:

• Patients with history of drug or alcohol abuse.
• Female patients who are pregnant or nursing (lactating).
• Patients with medical condition, laboratory abnormality, or psychiatric illness that, in the opinion of the investigator, might interfere with subject safety, compliance or evaluation of the condition of the study.
• Patients with positive blood screen for HIV, Hepatitis B (HbsAG) or Hepatitis C (HCV) virus.
• Patients with experience in any investigational drug in a clinical study within 6 months prior to study Day 1.
• Patients has a difficulty fasting or consuming standard meals.
• Patients has history of difficulties in swallowing or any gastrointestinal disease which could affect the drug absorption.
• Patients does not agree to not be engaged in strenuous exercise at least one day prior to study drug administration until donating the last sample of the study.
• Patients does not agree to not consuming any beverages or food containing grapefruit for at least two weeks prior to first study drug administration until donating the last sample of the study.
• Patients does not agree to not consuming any beverages or food containing methyl-xanthines e.g., caffeine (coffee, tea, cola, energy drinks, chocolate etc.) at least 48 hours prior to first study drug administration until donating the last sample of the study.
• Patients does not agree to not consuming any alcohol containing beverages and food at least 48 hours prior to first study drug administration until donating the last sample of the study

Sponsors & Collaborators

• Hikma Pharmaceuticals LLC: lead

Study Sites (1)

King Faisal Specialist Hospital and Research Centre

Riyadh, Saudi Arabia

Location

MeSH Terms

Conditions

Leukemia, Myeloid, Acute

Interventions

Azacitidine

Condition Hierarchy (Ancestors)

Leukemia, Myeloid; Leukemia; Neoplasms by Histologic Type; Neoplasms; Hematologic Diseases; Hemic and Lymphatic Diseases

Intervention Hierarchy (Ancestors)

Aza Compounds; Organic Chemicals; Cytidine; Pyrimidine Nucleosides; Pyrimidines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Nucleosides; Nucleic Acids, Nucleotides, and Nucleosides; Ribonucleosides

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: OTHER
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 11, 2024
• First Posted: March 22, 2024
• Study Start: May 2, 2024
• Primary Completion: August 17, 2025
• Study Completion: August 28, 2025
• Last Updated: September 26, 2025

Record last verified: 2024-03

Data Sharing

• IPD Sharing: Will not share

Locations

SA (1)