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A Phase I Clinical Trial to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of KR23248 Capsules in Healthy Adult Subjects

12. Mai 2026 aktualisiert von: Jiangxi Kvvit Pharmaceutical Co., Ltd.

A Randomized, Double-blind, Placebo-controlled, Dose-escalating Phase I Clinical Trial to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of Single and Multiple Doses of KR23248 Capsules in Healthy Adult Subjects

This study aims to investigate the safety, tolerability and pharmacokinetic characteristics of KR23248 capsules in healthy subjects. This study will be conducted in China. It will enroll male and female participants aged 18 years to 45 years.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Detaillierte Beschreibung

This study is a randomized, double-blind, placebo-controlled, dose-escalating Phase I trial, aiming to evaluate the safety, tolerability, and pharmacokinetic (PK) profiles of single and multiple oral doses of KR23248 capsules in healthy adult subjects. The study consists of two parts: Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) studies.

The single ascending dose study plans to enroll 54 healthy subjects, with predefined dose escalation levels of 0.5 mg, 1.0 mg, 2.0 mg, 3.0 mg, 4.5 mg, and 6.0 mg in sequence. The multiple ascending dose study sets the initial dose at 2.0 mg, with 12 healthy subjects planned for enrollment.

Studientyp

Interventionell

Einschreibung (Geschätzt)

66

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

  • Name: Huafang Li
  • Telefonnummer: +8618017311256
  • E-Mail: lhlh_5@163.com

Studieren Sie die Kontaktsicherung

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. Healthy male/female subjects aged ≥ 18 years and ≤ 45 years (inclusive) at the time of signing the informed consent form.
  2. Body Mass Index (BMI) ranging from 18.5 to 28.0 kg/m² (inclusive) at screening; male subjects with body weight ≥50 kg and female subjects with body weight ≥45 kg.
  3. Subjects who voluntarily participate in the trial and sign the informed consent form after understanding the purpose, content, procedures, and potential risks of the trial.
  4. Subjects who can communicate well with the investigators, are willing and able to comply with lifestyle restrictions specified in the protocol, and cooperate with study procedures.

Exclusion Criteria:

  1. Subjects with any diseases or dysfunctions in present illness and medical history that may interfere with the clinical trial, including but not limited to neurological and psychiatric diseases, cardiovascular diseases (e.g., congenital long QT syndrome), urinary system disorders, digestive system disorders, respiratory system disorders, musculoskeletal system disorders, metabolic and endocrine system disorders, skin diseases, hematological diseases, immune system diseases, and tumors.
  2. Subjects with any surgical condition or medical history that may significantly affect drug absorption, distribution, metabolism and excretion, or may pose a risk to the subject participating in the trial; such as a history of gastrointestinal surgery (gastrectomy, gastroenterostomy, enterectomy, etc.), urinary tract obstruction or dysuria, gastroenteritis, peptic ulcer, and history of gastrointestinal bleeding.
  3. Subjects with a history of severe allergic reactions or known hypersensitivity to any ingredients of the investigational product.
  4. Subjects with current or previous psychiatric disorders or cerebral dysfunction; those assessed to be at suicide risk based on the Columbia-Suicide Severity Rating Scale (C-SSRS), or by the investigator's clinical assessment, or those with a history of self-harm behavior.
  5. Subjects with a history of substance abuse within 1 year prior to administration or with a positive urine drug screening result.
  6. Subjects with a history of alcohol abuse within 6 months prior to screening (i.e., more than 14 standard units per week; 1 standard unit = 360 mL beer, or 45 mL spirits with 40% alcohol content, or 150 mL wine); or with a positive breath alcohol test; or unwilling to abstain from alcohol and any alcohol-containing products from screening until the last PK blood collection.
  7. Subjects with a history of surgery within 3 months prior to screening, or who have not recovered from surgery, or have a planned surgery scheduled during the trial.
  8. Subjects who have donated blood or experienced blood loss ≥ 400 mL within 3 months prior to screening, or ≥ 200 mL within one month, or have a history of blood product transfusion.
  9. Subjects who have participated in any clinical trial and received investigational drugs or medical devices within 3 months prior to screening.
  10. Subjects who have received vaccination within 30 days prior to screening, or have a vaccination plan during the entire study period.
  11. Subjects who have taken any medications within 28 days or 5 half-lives (whichever is longer) prior to screening and during the entire study period, including prescription drugs, over-the-counter drugs, herbal medicines, and any drugs that inhibit or induce hepatic drug-metabolizing enzymes (e.g., inducers and/or inhibitors of CYP3A4, CYP2D6, and CYP3A5).
  12. Female subjects who are pregnant, breastfeeding, or have a positive pregnancy test; or those who refuse to adopt effective non-pharmacological contraceptive measures (e.g., abstinence, intrauterine device, condoms with vaginal spermicide) throughout the study period and within 28 days after the end of administration; or those with a plan to donate sperm or ova.
  13. Subjects with clinically significant abnormal findings judged by the investigator in comprehensive physical examination, vital signs, laboratory tests and 12-lead electrocardiogram; including but not limited to: QTc > 450 ms in males and > 470 ms in females (Fridericia correction); resting pulse rate < 55 beats/min or > 100 beats/min; systolic blood pressure < 90 mmHg or ≥ 140 mmHg; diastolic blood pressure < 60 mmHg or ≥ 90 mmHg.
  14. Subjects with non-negative results for Hepatitis B surface antigen (HBsAg), Hepatitis C antibody (HCV-Ab), Human Immunodeficiency Virus antibody (HIV-Ab), and Toluidine Red Untreated Serum Test (TRUST).
  15. Subjects with alanine transaminase (ALT), creatinine (Cr) or serum prolactin level exceeding 2 times the upper limit of normal during the screening period.
  16. Subjects who smoke an average of ≥ 5 cigarettes per day within 3 months prior to screening, or are unable to abstain from any tobacco products during the trial.
  17. Subjects with an average daily intake of ≥ 5 cups of coffee or tea (200 mL per cup) within 3 months prior to screening, or are unable to discontinue intake during the trial.
  18. Subjects with special dietary requirements who cannot follow a unified study diet, or have difficulty in swallowing.
  19. Subjects who have consumed food or beverages containing grapefruit and/or pomelo within 7 days prior to administration.
  20. Subjects who have consumed xanthine-rich food or beverages (e.g., tea, coffee, cola, chocolate) within 3 days prior to administration.
  21. Subjects with poor compliance or other conditions deemed unsuitable for participation in the trial by the investigator.

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: Doppelt

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Part 1 cohort 1
SAD Cohort 1: single oral dose of 0.5mg KR23248 capsule
Participants will recieve a single oral dose of KR23248
Andere Namen:
  • KR23248 capsule
Experimental: Part 1 cohort 2
SAD Cohort 2: single oral dose of 1.0mg KR23248 capsule
Participants will recieve a single oral dose of KR23248
Andere Namen:
  • KR23248 capsule
Experimental: Part 1 cohort 3
SAD Cohort 3: single oral dose of 2.0mg KR23248 capsule
Participants will recieve a single oral dose of KR23248
Andere Namen:
  • KR23248 capsule
Experimental: Part 1 cohort 4
SAD Cohort 4: single oral dose of 3.0mg KR23248 capsule
Participants will recieve a single oral dose of KR23248
Andere Namen:
  • KR23248 capsule
Experimental: Part 1 cohort 5
SAD Cohort 5: single oral dose of 4.5mg KR23248 capsule
Participants will recieve a single oral dose of KR23248
Andere Namen:
  • KR23248 capsule
Experimental: Part 1 cohort 6
SAD Cohort 6: single oral dose of 6.0mg KR23248 capsule
Participants will recieve a single oral dose of KR23248
Andere Namen:
  • KR23248 capsule
Placebo-Komparator: Part 1 cohort 7
SAD cohort 7: single oral dose of placebo capsule
Teilnehmer erhalten Placebo
Andere Namen:
  • Placebo-Kapsel
Experimental: Part 2 KR23248 2.0mg
MAD: Multiple oral doses of 2.0mg KR23248 capsules administered once daily for 14 consecutive days
Participants will recieve a single oral dose of KR23248
Andere Namen:
  • KR23248 capsule
Placebo-Komparator: Part 2 Placebo
MAD: Multiple oral doses of placebo capsules administered once daily for 14 consecutive days
Teilnehmer erhalten Placebo
Andere Namen:
  • Placebo-Kapsel

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence of adverse events (AEs), serious adverse events(SAEs), drug-related AEs, and AEs leading to study withdrawal
Zeitfenster: SAD:Day 1 to Day14 MAD:Day1 to Day28
The number and percentage of participants with AEs,SAEs, drug-related AEs, and AEs leading to study withdrawal will be determined
SAD:Day 1 to Day14 MAD:Day1 to Day28

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Cmax
Zeitfenster: SAD:Day 1 to Day14 MAD:Day1 to Day28
Maximum Serum Concentration
SAD:Day 1 to Day14 MAD:Day1 to Day28
Tmax
Zeitfenster: SAD:Day 1 to Day14 MAD:Day1 to Day28
Time to Reach the Maximum Serum Concentration
SAD:Day 1 to Day14 MAD:Day1 to Day28
t1/2
Zeitfenster: SAD:Day 1 to Day14 MAD:Day1 to Day28
Elimination half-life
SAD:Day 1 to Day14 MAD:Day1 to Day28
λz
Zeitfenster: SAD:Day 1 to Day14 MAD:Day1 to Day28
Terminal rate constant
SAD:Day 1 to Day14 MAD:Day1 to Day28
AUC0-t
Zeitfenster: SAD:Day 1 to Day14 MAD:Day1 to Day28
Area under the plasma concentration-time curve from time zero to the last quantifiable concentration
SAD:Day 1 to Day14 MAD:Day1 to Day28
AUC0-∞
Zeitfenster: SAD:Day 1 to Day14 MAD:Day1 to Day28
Area under the plasma concentration-time curve from time zero extrapolated to infinity
SAD:Day 1 to Day14 MAD:Day1 to Day28
CL/F
Zeitfenster: SAD:Day 1 to Day14 MAD:Day1 to Day28
Apparent Clearance
SAD:Day 1 to Day14 MAD:Day1 to Day28
Vd/F
Zeitfenster: SAD:Day 1 to Day14 MAD:Day1 to Day28
Apparent Volume of Distribution
SAD:Day 1 to Day14 MAD:Day1 to Day28
MRT
Zeitfenster: SAD: Day1 to D14 MAD:Day1 to Day28
Mean residence time
SAD: Day1 to D14 MAD:Day1 to Day28
Css_min
Zeitfenster: MAD:Day1 to Day28
Steady-state trough concentration
MAD:Day1 to Day28
Css_max
Zeitfenster: MAD:Day1 to Day28
Steady-state peak concentration
MAD:Day1 to Day28
Tss,max
Zeitfenster: MAD:Day1 to Day28
Time to Reach Maximum Concentration at Steady State
MAD:Day1 to Day28
Cavg,ss
Zeitfenster: MAD:Day1 to Day28
Average Steady-State Concentration
MAD:Day1 to Day28
DF
Zeitfenster: MAD:Day1 to Day28
Fluctuation Percentage
MAD:Day1 to Day28
Rac
Zeitfenster: MAD:Day1 to Day28
Accumulation Factor
MAD:Day1 to Day28
AUCss
Zeitfenster: MAD:Day1 to Day28
Area under the plasma concentration-time curve over a dosing interval at steady state
MAD:Day1 to Day28

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

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)

19. Mai 2026

Primärer Abschluss (Geschätzt)

1. November 2026

Studienabschluss (Geschätzt)

1. November 2026

Studienanmeldedaten

Zuerst eingereicht

7. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

7. Mai 2026

Zuerst gepostet (Tatsächlich)

13. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

15. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

12. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • KR23248-202509

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

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