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The Safety and PK Study of Inhaled ICF004 in Healthy Chinese Volunteers (ICF004-INH)

17. Juli 2026 aktualisiert von: Jieming QU, Ruijin Hospital

A Randomized, Double-Blind, Placebo-Controlled Phase 1 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Inhaled Doses of ICF004 in Healthy Chinese Participants

The goal of this clinical trial is to learn about the safety of an inhaled study drug called ICF004 in healthy adults. ICF004 is being created to treat progressive lung scarring in the future. It will also learn how the body handles the drug over time.

The main questions it aims to answer are:

What medical problems or side effects do participants have when taking ICF004? How does the body absorb and metabolize ICF004? Researchers will compare ICF004 to a placebo (a look-alike powder that contains no active drug) to see if ICF004 is safe and well-tolerated.

Participants will:

Breathe in a single dose or multiple doses of ICF004 or a placebo using a dry powder inhaler; Stay at or visit the study clinic for checkups and tests; Give blood samples so researchers can measure the amount of drug in their blood.

Studienübersicht

Detaillierte Beschreibung

This is a randomized, double-blind, placebo-controlled Phase 1 study of ICF004 dry powder for inhalation in healthy Chinese adult participants. The study will evaluate the safety, tolerability, and plasma pharmacokinetics (PK) of ICF004 after single and multiple inhaled doses.

ICF004 is being developed as a potential treatment for progressive fibrosing interstitial lung disease (PF-ILD). PF-ILD includes interstitial lung diseases in which lung fibrosis continues to worsen. This progression may lead to worsening respiratory symptoms, declining lung function, and increasing fibrosis on high-resolution computed tomography. Current treatment options remain limited.

Preclinical studies suggest that ICF004 may affect signaling pathways involved in fibrosis, including pathways related to transforming growth factor beta 1 (TGF-beta 1). These effects may lower the abnormal deposition of collagen and other extracellular matrix components in the lungs. Administration by inhalation is intended to deliver ICF004 directly to the lungs. This route may achieve higher local lung exposure with a lower administered dose while limiting systemic exposure.

The study consists of a single ascending dose (SAD) part and a multiple ascending dose (MAD) part. Approximately 73 healthy male and female participants will be enrolled. Eligible participants will be 18 to 50 years of age and able to use the dry powder inhalation device correctly.

In each part, participants will be randomly assigned to receive ICF004 or matching placebo. The matching placebo will be administered using the same type of dry powder inhalation device. Participants, investigators, and other applicable study personnel will remain blinded to treatment assignment.

Part 1: Single Ascending Dose

The SAD part will evaluate the safety, tolerability, and plasma PK of ICF004 after a single inhaled dose. Approximately 41 participants will be enrolled across 5 sequential dose cohorts:

Cohort 1: 1 mg, with 3 participants randomized to ICF004 or placebo in a 2:1 ratio.

Cohort 2: 4 mg, with 10 participants randomized to ICF004 or placebo in a 4:1 ratio.

Cohort 3: 8 mg, with 10 participants randomized to ICF004 or placebo in a 4:1 ratio.

Cohort 4: 12 mg, with 10 participants randomized to ICF004 or placebo in a 4:1 ratio.

Cohort 5: 16 mg, with 8 participants randomized to ICF004 or placebo in a 3:1 ratio.

Participants will enter the clinical study unit on Day -1 and receive a single dose of ICF004 or placebo on Day 1. Participants may leave the study unit on Day 2 after completing the required assessments. They will return for safety assessments on Day 4. Researchers will conduct a telephone follow-up on Day 7 to collect information about adverse events and concomitant medications or treatments.

Safety assessments in the SAD part will include adverse event monitoring, local irritation assessments, vital signs, physical examinations, clinical laboratory tests, 12-lead electrocardiograms, and pulmonary function tests. Local irritation monitoring will include symptoms such as cough, wheezing, chest tightness, sore throat, choking, itchy throat, and a feeling of a foreign object in the throat.

Blood samples for plasma PK assessment will be collected within 1 hour before dosing and at 5, 10, 20, 30, and 45 minutes after dosing. Additional samples will be collected at 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after dosing.

The SAD PK assessments will include maximum observed plasma concentration (Cmax), time to maximum observed plasma concentration (Tmax), area under the plasma concentration-time curve (AUC), terminal elimination half-life, terminal elimination rate constant, apparent clearance, apparent volume of distribution, mean residence time, and the percentage of AUC extrapolated to infinity.

Part 2: Multiple Ascending Dose

The MAD part will evaluate the safety, tolerability, and plasma PK of ICF004 after repeated inhaled doses. The dose levels and dry powder inhalation regimen used in this part may be adjusted based on available results from the SAD part.

Approximately 32 participants will be enrolled across 4 planned MAD cohorts. Two cohorts are planned to receive study treatment once daily (QD), and two cohorts are planned to receive study treatment twice daily (BID). Each cohort will include 8 participants randomized in a 6:2 ratio to receive ICF004 or matching placebo.

Participants will receive multiple inhaled doses from Day 1 through Day 7. Participants in the QD cohorts will receive study treatment once daily. Participants in the BID cohorts will generally receive study treatment twice daily. On Day 7, participants in the BID cohorts will receive only the morning dose, which will be their last dose.

Participants may leave the clinical study unit on Day 8 after completing the required assessments. They will return for additional safety assessments on Day 11. Researchers will conduct a telephone follow-up on Day 14 to collect information about adverse events and concomitant medications or treatments.

Safety assessments in the MAD part will include adverse event monitoring, local irritation assessments after dosing, vital signs, physical examinations, clinical laboratory tests, 12-lead electrocardiograms, pulmonary function tests, and other protocol-specified assessments. Local irritation will be monitored for 4 hours after each dose.

For the QD cohorts, intensive plasma PK samples will be collected before and through 24 hours after the first dose on Day 1. Additional predose samples will be collected on Days 3 through 7. After the last dose on Day 7, intensive PK samples will be collected through 24 hours post-dose.

For the BID cohorts, intensive plasma PK samples will be collected before and through 12 hours after the first dose on Day 1. The 12-hour sample will be collected before the second dose. Additional samples will be collected before the morning doses on Days 3 through 7. The Day 7 morning dose will be the last dose. Intensive PK samples will then be collected through 24 hours after that dose.

Each scheduled PK blood sample will have a volume of approximately 4 mL. When applicable, an additional PK sample may be collected if a participant withdraws early or discontinues study treatment. Plasma samples will be processed and managed according to the study laboratory manual.

The MAD PK assessments will include PK parameters after the first dose and after the last dose. First-dose parameters will include Cmax, Tmax, and AUC. Multiple-dose and steady-state parameters will include maximum, average, and trough plasma concentrations; time to maximum plasma concentration; AUC to the last measurable concentration; AUC over a dosing interval; AUC extrapolated to infinity; terminal elimination half-life; terminal elimination rate constant; apparent clearance; apparent volume of distribution; degree of fluctuation; peak-to-trough swing; and accumulation ratios based on Cmax and AUC.

Safety Evaluation

The primary safety outcome is the occurrence of treatment-emergent adverse events (TEAEs). A TEAE is an adverse event that begins or worsens after the first dose of ICF004 or placebo. Researchers will monitor TEAEs from Day 1 through Day 7 in the SAD part and from Day 1 through Day 14 in the MAD part.

Safety findings may include local irritation symptoms and clinically significant abnormalities identified through clinical laboratory tests, 12-lead electrocardiograms, pulmonary function tests, vital signs, or physical examinations. The investigator will determine the clinical significance of abnormal findings and whether they should be recorded as adverse events.

The study is designed to characterize the safety, tolerability, and plasma PK of ICF004 in healthy participants. It is not designed to evaluate whether ICF004 treats PF-ILD or any other disease.

Studientyp

Interventionell

Einschreibung (Geschätzt)

73

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

Inclusion Criteria:

  1. Fully understand the study procedures and methods, volunteer to participate in this study, and sign the written informed consent form.
  2. Healthy adult participants, male or female, aged 18 to 50 years (inclusive).
  3. Body Mass Index (BMI) ≥ 18 and < 28 kg/m²; body weight ≥ 50.0 kg and < 90.0 kg for males, and ≥ 45.0 kg and < 90.0 kg for females.
  4. Medically healthy as determined by the investigator, based on the absence of clinically significant abnormalities in physical examinations, laboratory tests, vital signs, chest X-ray, and electrocardiogram (ECG).
  5. Able to use the inhalation device correctly and effectively.
  6. Agree to use effective contraceptive measures throughout the study period. Female participants of childbearing potential must agree to use effective contraception from the screening period until 6 months after the last dose. During this period, female participants must agree to have no plans for pregnancy or egg donation/harvesting; male participants must agree to have no plans to father a child or donate sperm. Their male or female partners of childbearing potential must also agree to use effective contraceptive measures during this period.

Exclusion Criteria:

  1. History of any clinically significant disease (including past and current history), including but not limited to respiratory, cardiovascular, gastrointestinal, hematological, endocrine, immunological, dermatological, malignant tumor, neuropsychiatric, ear/nose/throat (ENT), or metabolic diseases; or any other condition that, in the opinion of the investigator (or sub-investigator), makes the participant unsuitable for the study.
  2. Major surgery within 6 months prior to dosing, planned surgery during the study, or previous surgery that may significantly affect the pharmacokinetics or safety evaluation of the study drug.
  3. Current oral diseases that may affect the study, as judged by the investigator (e.g., oropharyngeal candidiasis, oral ulcers, oral mucosal lesions).
  4. Fever (body temperature > 37.5°C) or symptomatic respiratory infection within 1 month prior to dosing; any infection requiring systemic antibiotics or antivirals within 3 months prior to screening; or a history of recurrent infections.
  5. Positive test results for Human Immunodeficiency Virus (HIV), Hepatitis B surface antigen (HBsAg), Treponema pallidum (syphilis) antibody, or Hepatitis C Virus (HCV) antibody.
  6. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyl transferase (GGT), or total bilirubin exceeding the upper limit of normal (ULN) at the screening or baseline visit.
  7. Forced expiratory volume in 1 second (FEV1) and forced vital capacity (FVC) < 80% of the predicted value, or FEV1/FVC < 0.7, or arterial oxygen saturation < 95% at the screening or baseline visit.
  8. Smoking (including e-cigarettes) within 6 months prior to dosing, or a positive smoking (nicotine/cotinine) test.
  9. History of drug abuse within 3 months prior to screening, or a positive urine drug screen.
  10. Participation in any drug or medical device clinical trial within 3 months prior to screening.
  11. Blood donation or blood loss ≥ 400 mL within 3 months prior to dosing.
  12. Difficulty in venous blood sampling, intolerance to venipuncture, or a history of needle or blood phobia (vasovagal syncope).
  13. Known allergy to the study drug or any of its ingredients.
  14. Female participants who are pregnant or lactating, or who plan to become pregnant from the time of the study through 6 months after the last dose.
  15. Any condition that, in the opinion of the investigator, makes the participant unsuitable for participation in the study.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Part 1 (SAD): ICF004
Participants in the Single Ascending Dose (SAD) part will receive a single dose of ICF004 via dry powder inhaler. There are 5 planned dose cohorts (1, 4, 8, 12, and 16 mg).
Participants in the Multiple Ascending Dose (MAD) part will receive multiple doses of ICF004 via dry powder inhaler. The doses will be administered once daily (QD) or twice daily (BID). There are 4 planned cohorts. The exact dose levels will be determined based on the safety and tolerability results from Part 1.
Placebo-Komparator: Part 1 (SAD): Placebo
Participants in the Single Ascending Dose (SAD) part will receive a single dose of matching placebo via dry powder inhaler.
Experimental: Part 2 (MAD): ICF004
Participants in the Single Ascending Dose (SAD) part will receive a single dose of ICF004 via dry powder inhaler. There are 5 planned dose cohorts (1, 4, 8, 12, and 16 mg).
Participants in the Multiple Ascending Dose (MAD) part will receive multiple doses of ICF004 via dry powder inhaler. The doses will be administered once daily (QD) or twice daily (BID). There are 4 planned cohorts. The exact dose levels will be determined based on the safety and tolerability results from Part 1.
Placebo-Komparator: Part 2 (MAD): Placebo
Participants in the Multiple Ascending Dose (MAD) part will receive multiple doses of matching placebo via dry powder inhaler, administered once daily (QD) or twice daily (BID).

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of Participants with Treatment-Emergent Adverse Events (TEAEs)
Zeitfenster: Day 1 through Day 7 for SAD and Day 1 through Day 14 for MAD
A treatment-emergent adverse event (TEAE) is an adverse event that begins or worsens after the first dose of ICF004 or placebo. Safety assessments include local irritation symptoms, clinical laboratory tests, 12-lead electrocardiograms, pulmonary function tests, vital signs, and physical examinations. Clinically significant abnormal findings may be recorded as adverse events, as determined by the investigator.
Day 1 through Day 7 for SAD and Day 1 through Day 14 for MAD

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Cmax: Maximum Observed Plasma Concentration After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Tmax: Time to Maximum Observed Plasma Concentration After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
AUC0-t: Area Under the Plasma Concentration-Time Curve From Time Zero to the Last Measurable Concentration After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
AUC0-♾️: Area Under the Plasma Concentration-Time Curve From Time Zero to Infinity After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
t1/2z: Terminal Elimination Half-Life After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
λz: Terminal Elimination Rate Constant After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
CLz/F: Apparent Total Clearance After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Vd/F: Apparent Volume of Distribution During the Terminal Phase After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
MRT: Mean Residence Time After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
AUCE_%Extrap: Percentage of AUC0-♾️ Extrapolated From the Last Measurable Concentration to Infinity After a Single Dose
Zeitfenster: Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after a single inhaled dose.
Predose; 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours post-dose.
Cmax: Maximum Observed Plasma Concentration After the First Dose
Zeitfenster: At 0 hour (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, and 12 hours post-dose; additionally at 24 hours post-dose for the once-daily cohorts.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after the first inhaled dose.
At 0 hour (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, and 12 hours post-dose; additionally at 24 hours post-dose for the once-daily cohorts.
Tmax: Time to Maximum Observed Plasma Concentration After the First Dose
Zeitfenster: At 0 hour (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, and 12 hours post-dose; additionally at 24 hours post-dose for the once-daily cohorts.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after the first inhaled dose.
At 0 hour (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, and 12 hours post-dose; additionally at 24 hours post-dose for the once-daily cohorts.
AUC0-t: Area Under the Plasma Concentration-Time Curve From Time Zero to the Last Measurable Concentration After the First Dose
Zeitfenster: At 0 hour (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, and 12 hours post-dose; additionally at 24 hours post-dose for the once-daily cohorts.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after the first inhaled dose.
At 0 hour (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, and 12 hours post-dose; additionally at 24 hours post-dose for the once-daily cohorts.
Ctrough,ss: Trough Plasma Concentration at Steady State
Zeitfenster: At 0 hour (within 1 hour before the morning dose) on Days 3, 4, 5, 6, and 7.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses. Samples will be collected before the morning dose on Days 3 through 7.
At 0 hour (within 1 hour before the morning dose) on Days 3, 4, 5, 6, and 7.
Cmax,ss: Maximum Observed Plasma Concentration After the Last Dose
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses. The Day 7 morning dose is the last dose for both the once-daily and twice-daily cohorts.
At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Tmax,ss: Time to Maximum Observed Plasma Concentration After the Last Dose
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses. The Day 7 morning dose is the last dose for both the once-daily and twice-daily cohorts.
At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Cav,ss: Average Plasma Concentration at Steady State
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses.
At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
AUC0-t,ss: Area Under the Plasma Concentration-Time Curve From Time Zero to the Last Measurable Concentration After the Last Dose
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses.
At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
AUC0-tau,ss: Area Under the Plasma Concentration-Time Curve Over a Dosing Interval at Steady State
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose) through 24 hours after the last dose for the once-daily cohorts, and through 12 hours after the last dose for the twice-daily cohorts.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses. The dosing interval is 24 hours for the once-daily cohorts and 12 hours for the twice-daily cohorts.
At 0 hour on Day 7 (within 1 hour predose) through 24 hours after the last dose for the once-daily cohorts, and through 12 hours after the last dose for the twice-daily cohorts.
AUC0-♾️: Area Under the Plasma Concentration-Time Curve From Time Zero to Infinity After the Last Dose
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses.
At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
t1/2: Terminal Elimination Half-Life After the Last Dose
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses.
At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
λz: Terminal Elimination Rate Constant After the Last Dose
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses.
At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
CLss/F: Apparent Clearance at Steady State
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses.
At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Vd/F: Apparent Volume of Distribution During the Terminal Phase After the Last Dose
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses.
At 0 hour on Day 7 (within 1 hour predose); 5, 10, 20, 30, and 45 minutes; and 1, 1.5, 2, 3, 4, 6, 8, 10, 12, and 24 hours after the last dose.
DF: Degree of Fluctuation at Steady State
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose) through 24 hours after the last dose for the once-daily cohorts, and through 12 hours after the last dose for the twice-daily cohorts.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses.
At 0 hour on Day 7 (within 1 hour predose) through 24 hours after the last dose for the once-daily cohorts, and through 12 hours after the last dose for the twice-daily cohorts.
Swing: Peak-to-Trough Fluctuation at Steady State
Zeitfenster: At 0 hour on Day 7 (within 1 hour predose) through 24 hours after the last dose for the once-daily cohorts, and through 12 hours after the last dose for the twice-daily cohorts.
Plasma pharmacokinetic (PK) parameter of ICF004 in healthy Chinese participants after multiple inhaled doses.
At 0 hour on Day 7 (within 1 hour predose) through 24 hours after the last dose for the once-daily cohorts, and through 12 hours after the last dose for the twice-daily cohorts.
Rcmax: Accumulation Ratio Based on Maximum Plasma Concentration
Zeitfenster: From the first dose on Day 1 through 24 hours after the last dose on Day 7.
Plasma pharmacokinetic (PK) parameter of ICF004 calculated from the maximum plasma concentrations after the first and last inhaled doses.
From the first dose on Day 1 through 24 hours after the last dose on Day 7.
RAUC: Accumulation Ratio Based on Area Under the Plasma Concentration-Time Curve
Zeitfenster: From the first dose on Day 1 through 24 hours after the last dose on Day 7.
Plasma pharmacokinetic (PK) parameter of ICF004 calculated from the plasma concentration-time curves after the first and last inhaled doses.
From the first dose on Day 1 through 24 hours after the last dose on Day 7.

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Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

30. Juli 2026

Primärer Abschluss (Geschätzt)

30. Juli 2029

Studienabschluss (Geschätzt)

30. Juli 2029

Studienanmeldedaten

Zuerst eingereicht

14. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

17. Juli 2026

Zuerst gepostet (Tatsächlich)

22. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

22. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

17. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • nIC004-202508

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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