Safety and Pharmacokinetics Study of Multiple Ascending Doses of VV261 Tablets
A Phase I Clinical Study Evaluating the Safety, Tolerability, Pharmacokinetics of a Multiple Oral Dose of VV261 Tablets in Chinese Healthy Participants.
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Phase 1
Kontakte und Standorte
Studienkontakt
Studienkontakt
- Name: Huaqing Duan
- Telefonnummer: 18061926005
- E-Mail: huaqing.duan@vigonvita.cn
Studienorte
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Anhui
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Hefei, Anhui, China, 230031
- The First Affiliated Hospital of Anhui Medical University
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Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Aged 18 to 45 years old, males or females;
- Males weight no less than 50 kg, females weight no less than 45 kg, with body mass index of 19 to 26 kg/m^2;
- Vital signs examination, physical examination, laboratory examination ,electrocardiogram examination chest CT and B-ultrasound of liver, gallbladder, pancreas, spleen, kidney and thyroid results are normal or considered abnormal without clinical significance by the investigator;
- Participants who are willing to take proper contraceptive methods during the study and within 3 months after the the last administration;
- Participants who are able to understand and follow the study protocol and instructions; participants who have voluntarily decided to participate in this study, and sign the informed consent form.
Exclusion Criteria:
- Participants with hypersensitivity to preparation or any of the excipients;
- Participants with allergic constitution (such as asthma, urticaria, eczematous dermatitis and other allergic diseases), or have a history of drug or food allergy;
- Participants with central nervous system, cardiovascular system, gastrointestinal, respiratory system, urinary, hematologic, or metabolic disorders that require medical intervention or other diseases (such as psychiatric history) that are not suitable for clinical trials;participants with a history of gastrointestinal conditions that may impair drug absorption (e.g., gastrectomy or small intestine resection, atrophic gastritis, gastrointestinal ulcers or perforations/fistulas, gastrointestinal bleeding, or obstruction);participants with previous surgery that may significantly affect the body's metabolic process or safety evaluation of the study drug (such as liver, gallbladder, kidney, splenectomy, gastrointestinal resection or excessive blood loss that affects drug absorption, distribution, metabolism)
- Participants with a history of diseases affecting bone marrow hematopoietic function or reducing immunological function (including leukemia, myelodysplastic syndrome, aplastic anemia, systemic lupus erythematosus, rheumatoid arthritis, etc.) or treatment history (tumor chemotherapy or radiotherapy, use of immunosuppressants, etc.);
- Participants with a history of spleen diseases;
- If any of the following parameters were considered abnormal with clinical significance: white blood cell count, red blood cell count, platelet count, reticulocyte count, and absolute neutrophil count;
- If any of the following parameters were considered abnormal with clinical significance: total bilirubin, alkaline phosphatase, alanine aminotransferase, and aspartate aminotransferase;
- Participants who have received blood transfusion or used blood products within 3 months before screening or who have lost more than ≥400 mL of blood due to other reasons (excluding menstruation);
- Participants who have participated in clinical trials and received drugs within 3 months before screening;
- Participants who have taken any prescription drugs, over-the-counter drugs, Chinese herbal medicines or health products within 2 weeks before screening;
- Participants who have received vaccination within the first 2 weeks before screening, or planned to receive any vaccine during the trial or within 1 week after the end of the study;
- Participants with a history of drug abuse within 1 year before screening or positive urine drug screening within 1 year before screening results (morphine, tetrahydrocannabinol, methamphetamine, dimethylene diphenazine , ketamine, and cocaine);
- Participants who drink more than 14 standard units or at least twice a day per week within one year before screening,(one standard unit equals 200 mL of beer with 5% alcohol or 25 mL of white wine with 40% alcohol content or 85 mL of red wine with 12% alcohol) or participants with breath alcohol test >0 mg/100 mL;
- Participants who smok more than 5 cigarettes a day within one year before screening;
- Participants who can't quit smoking or drinking during the trial period;
- Participants who are positive for hepatitis B virus surface antigen, hepatitis C virus antibody, treponema pallidum antibody or human immunodeficiency virus antibody (Anti-HIV);
- Participants who cannot tolerate blood collection with intravenous indwelling needles or blood fainting;
- Participants with lactose intolerance or cannot comply with a uniform diet (such as special dietary requirements, intolerance of standard meals, etc.), Participants who have consumed excessive amounts of strong tea, coffee or caffeinated beverages in the 3 months before screening;
- Participants with difficulty in swallowing tablets;
- Pregnant or lactating women; participants whose spouses or partners intend to become pregnant, plan sperm or oocyte donation within 3 months after the last dose, or decline to use acceptable effective contraception;
- The investigator believes that there are other unsuitable factors to participate this trial.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Doppelt
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
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Placebo-Komparator: Placebo
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6 participants receive VV261 100mg 6 tablets,three times daily,orally; 2 participants will receive placebo,orally
6 participants receive VV261 100mg 9 tablets,three times daily,orally; 2 participants will receive placebo,orally
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Experimental: VV261
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6 participants receive VV261 100mg 6 tablets,three times daily,orally; 2 participants will receive placebo,orally
6 participants receive VV261 100mg 9 tablets,three times daily,orally; 2 participants will receive placebo,orally
|
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Cmax
Zeitfenster: Baseline to 72 hours after the last administration
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Maximum observed plasma concentration
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Baseline to 72 hours after the last administration
|
|
Tmax
Zeitfenster: Baseline to 72 hours after the last administration
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Time at which Cmax occurs
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Baseline to 72 hours after the last administration
|
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Ctrough
Zeitfenster: Baseline to 72 hours after the last administration
|
Minimum observed steady-state plasma concentration
|
Baseline to 72 hours after the last administration
|
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AUC0-t
Zeitfenster: Baseline to 72 hours after the last administration
|
Area under the plasma concentration time curve from time zero to the last measurable concentration
|
Baseline to 72 hours after the last administration
|
|
AUC0-∞
Zeitfenster: Baseline to 72 hours after the last administration
|
Area under the plasma concentration-time curve from time zero to infinity
|
Baseline to 72 hours after the last administration
|
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t1/2
Zeitfenster: Baseline to 72 hours after the last administration
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Half life of elimination
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Baseline to 72 hours after the last administration
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CL/F
Zeitfenster: Baseline to 72 hours after the last administration
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Apparent clearance
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Baseline to 72 hours after the last administration
|
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mean Resident Time
Zeitfenster: Baseline to 72 hours after the last administration
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Mean Resident Time from time zero to infinity/the last
|
Baseline to 72 hours after the last administration
|
|
Vd/F
Zeitfenster: Baseline to 72 hours after the last administration
|
Apparent volume of distribution during the terminal phase
|
Baseline to 72 hours after the last administration
|
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Incidence of Treatment-Emergent Adverse Events
Zeitfenster: Baseline to 7days after the last administration
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Incidence of Treatment-Emergent Adverse Events
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Baseline to 7days after the last administration
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Mitarbeiter und Ermittler
Sponsor
Sponsor
Ermittler
Ermittler
- Hauptermittler: Huan Zhou, The First Affiliated Hospital of Anhui Medical University
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Studienbeginn
Primärer Abschluss (Geschätzt)
Primärer Abschluss
Studienabschluss (Geschätzt)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- VV261-02
Plan für individuelle Teilnehmerdaten (IPD)
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Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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