HMPL-689 Drug Interaction Study With CYP3A Inhibitor/CYP2C9 Inhibitor/CYP3A Inducer/PPI

NCT05602597 | Completed Phase 1 FDA Drug

• 1 other identifier: 2021-689-00US1
• Study Type: interventional
• Target: 59
• Locations: 1 country
• Sites: 1

Brief Summary

An open-label study to determine effect of Itraconazole, Fluconazole, Rifampin, and Rabeprazole on the PK of HMPL-689

Conditions

Relapsed or Refractory Lymphoma

Keywords

Itraconazole; Fluconazole; Rifampin; Rabeprazole

Outcome Measures

Primary Outcomes (3)

• AUC0-t

  Area under the plasma concentration-time curve from time 0 to time of the last measurable concentration

  From Day 1 to Day 11 (Day 12 for Rifampin)

• AUC0-inf

  Area under the plasma concentration-time curve from time 0 to infinity (if data permit)

  From Day 1 to Day 11 (Day 12 for Rifampin)

• Cmax

  Maximum observed plasma concentration

  From Day 1 to Day 11 (Day 12 for Rifampin)

Secondary Outcomes (1)

• Incidence of AEs/SAEs

  From Day 1 to Day 11 (Day 12 for Rifampin)

Study Arms (4)

Part A - Itraconazole

EXPERIMENTAL

Period 1 -- Participants to receive 10mg dose of HMPL-689 by mouth as a single agent treatment on Day 1 Period 2 -- Participants to receive 200mg Itraconazole by mouth twice daily beginning on Day 3 through Day 10. On Day 7 200 mg Itraconazole and 10 mg HMPL-689 will be simultaneously administered.

Drug: Itraconazole 200 mg

Part B - Fluconazole

EXPERIMENTAL

Period 1 -- Participants to receive 10mg dose of HMPL-689 by mouth as a single agent treatment on Day 1 Period 2 -- Participants to receive 400mg Fluconazole by mouth daily on Day 3, then 200 mg Fluconazole by mouth daily Day 4 through Day 10. On Day 7 200 mg Fluconazole and 10 mg HMPL-689 will be simultaneously administered.

Drug: Fluconazole 400 mg

Part C - Rimfampin

EXPERIMENTAL

Period 1 -- Participants to receive 30mg dose of HMPL-689 by mouth as a single agent treatment on Day 1 Period 2 -- Participants to receive 600mg Rifampin by mouth daily beginning on Day 3 through Day 11. On Day 10 600mg Rifampin will be administered by mouth approximately 1 hour before the start of breakfast and 30mg HMPL-689 will be administered by mouth approximately 30 minutes after the start of breakfast.

Drug: Rifampin 600 mg

Part D - Rabeprazole

EXPERIMENTAL

Period 1 -- Participants to receive 30mg dose of HMPL-689 by mouth as a single agent treatment on Day 1 Period 2 -- Participants to receive 40mg Rabeprazole by mouth daily beginning on Day 3 through Day 9. On Day 9 40mb Rabeprazole will be administered by mouth approximately 1 hour before the start of breakfast and 30mg HMPL-689 will be administered by mouth approximately 30 minutes after the start of breakfast.

Drug: Rabeprazole 40 mg

Interventions

Itraconazole 200 mg DRUG

Study participants will be administered 200 mg itraconazole by mouth twice daily after the pharmacokinetic blood draw on Day 3 and once daily on Days 4 to 10, inclusive.

Part A - Itraconazole

Fluconazole 400 mg DRUG

Study participants will be administered 400 mg fluconazole by mouth daily on Day 3 after the pharmacokinetic blood draw, and 200 mg fluconazole by mouth daily on Days 4 to 10, inclusive.

Part B - Fluconazole

Rifampin 600 mg DRUG

Study participants will be administered 600 mg rifampin by mouth daily starting on Day 3, after the pharmacokinetic blood draw, and on Days 4 to 11, inclusive.

Part C - Rimfampin

Rabeprazole 40 mg DRUG

Study participants will be administered 40 mg rabeprazole by mouth daily on Day 3, after the pharmacokinetic blood draw, and on Days 4 to 9, inclusive.

Part D - Rabeprazole

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Male or female between the ages of 18 and 55 years old (inclusive) at the time of informed consent.
• Body mass index (BMI) \>18 and ≤29.9 kg/m2 at screening.
• Females must be postmenopausal (defined as absence of menses for at least 1 year without alternative medical cause) or permanently sterile by total hysterectomy, bilateral oophorectomy, or bilateral salphingectomy.
• Males, including those who have had a successful vasectomy, must use a condom during sexual intercourse with women of childbearing potential starting from their first dose of study drug through 30 days after their last dose of study drug. Alternatively, abstinence is allowed if it is the normal and preferred lifestyle of the healthy volunteer.
• Must provide written informed consent prior to any study-specific screening procedures.
• Willing and able to comply with all aspects of the protocol, as determined by the PI.

You may not qualify if:

• Known history of any gastrointestinal surgery or any condition possibly affecting drug absorption (eg, cholecystectomy, gastrectomy, achlorhydria, peptic ulcer disease, history of stomach or intestinal surgery, or resection). Appendectomy and hernia repair are allowed.
• Clinically significant illness within 8 weeks or a clinically significant infection within 4 weeks prior to the first dose.
• Evidence of a clinically significant deviation from normal in the physical examination, vital signs, or clinical laboratory determinations at screening or at Day -1 Check-in (baseline).
• Systolic blood of pressure \>140 mmHg or diastolic blood pressure of \> 90 mmHg.
• Clinically significant ECG abnormality, including a marked baseline prolongation of QT/QTc interval (eg, repeated demonstration of a QTcF interval of \> 450 msec), or had a family history of prolonged QTc syndrome or sudden death.
• History of smoking or use of nicotine containing substances within the previous 2 months, as determined by medical history or healthy volunteer's verbal report and confirmed by cotinine test at check in for each treatment period.
• History of drug and/or alcohol misuse prior to screening or a positive urine drug test at Screening or at Check in for each treatment period.
• Diagnosed with acquired immune deficiency syndrome or has performed tests that are positive for human immunodeficiency virus, hepatitis B virus (HBV), hepatitis C virus (HCV), cytomegalovirus, or pneumocystis jiroveci pneumonia.
• Participated in a clinical trial of other drug before screening, and the time since the last use of other study drug is less than 5 times the half-life or 4 weeks, whichever is longer, or the healthy volunteer is currently enrolled in another clinical study.
• Consumed grapefruit, starfruit, Seville oranges, or their products within 7 days prior to the first dose.
• Consumed herbal preparations/medications, including, but not limited to, St. John's Wort, kava, ephedra (ma huang), Ginkgo biloba, dehydroepiandrosterone, yohimbe, saw palmetto, and ginseng, within 7 days prior to the first dose (21 days for St. John's Wort).
• Experienced a weight loss or gain of \>10% within 4 weeks prior to the first dose as noted by medical history and weight at screening and Check-in.
• Received blood or blood products within 4 weeks or donated blood or blood products within 8 weeks prior to the first dose or donated double red cell within 16 weeks prior to first dose.
• Used any over-the-counter (OTC) medications or prescription drugs (medications that can inhibit or induce CYP3A4/CYPC9, or lower gastric acid in particular) within 2 weeks prior to the first dose.
• Allergic to any of the study drugs (or its excipients) to be given in this study.

Sponsors & Collaborators

• Hutchmed: lead

Study Sites (1)

QPS- Miami

Miami, Florida, 33143, United States

Location

MeSH Terms

Conditions

Recurrence; Lymphoma

Interventions

Itraconazole; Fluconazole; Rifampin; Rabeprazole

Condition Hierarchy (Ancestors)

Disease Attributes; Pathologic Processes; Pathological Conditions, Signs and Symptoms; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Hemic and Lymphatic Diseases; Immunoproliferative Disorders; Immune System Diseases

Intervention Hierarchy (Ancestors)

Triazoles; Azoles; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Piperazines; Rifamycins; Heterocyclic Compounds, 4 or More Rings; Heterocyclic Compounds, Fused-Ring; Lactams, Macrocyclic; Macrocyclic Compounds; Polycyclic Compounds; 2-Pyridinylmethylsulfinylbenzimidazoles; Sulfoxides; Sulfur Compounds; Organic Chemicals; Pyridines; Benzimidazoles; Heterocyclic Compounds, 2-Ring

Study Officials

• Vijay Jayaprakash, MD

  Hutchmed

  STUDY DIRECTOR

Study Design

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

Study Record Dates

• First Submitted: October 27, 2022
• First Posted: November 2, 2022
• Study Start: June 1, 2022
• Primary Completion: August 6, 2022
• Study Completion: August 6, 2022
• Last Updated: March 6, 2024

Record last verified: 2024-03

Locations

US (1)