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Safety, Tolerability and Pharmacokinetics of RNV-166 in Healthy Male Volunteers

4. september 2026 oppdatert av: InVitro Research Solutions Private Limited

A Randomized, Double-Blind, Placebo-controlled, Single-Ascending-Dose and Multiple-Ascending-Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of RNV-166 in Healthy Male Volunteers

This Phase 1 first-in-human clinical study evaluated the safety, tolerability, and pharmacokinetics of RNV-166 following single ascending dose (SAD) and multiple ascending dose (MAD) administration in healthy participants. Single oral doses of RNV-166 ranging from 200 mg to 1600 mg were assessed, including evaluation under fed (high-fat meal) conditions to characterize food effects on pharmacokinetics. Multiple ascending doses were administered once daily for up to 28 days to assess safety, tolerability, and pharmacokinetic profile following repeated dosing.

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

66

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Rajshahi, Bangladesh, 6000
        • Rajshahi Medical College Hospital

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  1. Healthy Male subjects between 18 and 40 years of age (both inclusive).
  2. Healthy as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, laboratory tests, vital signs and ECG. A subject with a clinically significant abnormality or laboratory parameters significantly outside the reference range for the population being studied may be included only if according to the investigator's opinion, the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.
  3. AST, ALT, alkaline phosphatase and bilirubin ≤1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).
  4. Non-smoker and non-tobacco user.
  5. No history or current practice of alcohol/substance/drug use.
  6. No history of psychiatric disorders assessed by a clinical psychological evaluation and DSM V criteria.
  7. Body mass index (BMI) between 19 and 27 kg/m2 inclusive.
  8. Male subject with female partners of child-bearing potential must agree to use one of the contraception methods. Subjects with female partners of child-bearing potential must use condom while the female partner must use a highly effective contraceptive, such as IUD, birth control pills or diaphragm with spermicide, after the first dose of study treatment and until the end of study visit (for female partners) and during an additional 6 months from the last dose (for subjects themselves).
  9. Has a physical condition which enable patients to be fit for a pharmacokinetic sampling according to principal investigator evaluation.
  10. Be willing and able to comply with study procedures for the duration of the study.
  11. Able to understand and willing to sign written informed consent form.
  12. The subjects who are at present, and who can remain drug naïve for at least 14 days prior to dosing and till the end of the study, including herbal supplements, nutraceuticals.
  13. Refrain from taking grapefruit, grapefruit juice, orange fruit & orange juice during the study period

Exclusion Criteria:

  1. Female volunteers and male volunteers who are either <18 years or >40 years.
  2. History of asthma, anaphylaxis or anaphylactoid reactions, severe allergic responses.
  3. History of relevant atopy or drug hypersensitivity.
  4. Known allergy to any component of RNV-166 oral capsule or its placebo (HPMC or cellulose microcrystalline).
  5. History of major medical, psychiatric illness or surgery which, in the judgment of the investigator, puts them 'at risk' or is likely to modify their handling of the study drug.
  6. Acute or chronic systemic disease or disorder (respiratory, gastrointestinal, renal, hepatic, hematological, lymphatic, neurological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, dermatological, endocrine).
  7. Impaired renal function defined by a creatinine clearance < 90 mL/min calculated using the Cockcroft-Gault equation5 (FDA Guidance for Industry: Pharmacokinetics in patients with Impaired Renal Function, March 2010).
  8. History of nephritic colic and/or renal calculi.
  9. History of drug abuse and/or regular use of tobacco- or nicotine-containing products >5/day within three months of the study.
  10. History of alcohol consumption exceeding, (on average 21 drinks/week for men) within 6 months of the first dose of study medication.
  11. Drinking excessive amounts of tea, coffee, chocolate and/or beverage containing caffeine (> 4 cups / day).
  12. Vital signs with a clinically significant abnormality at screening.
  13. ECG with a clinically significant abnormality at screening.
  14. Laboratory test values outside the clinically acceptable 'normal range' for healthy volunteers at screening.
  15. Positive HIV, Hepatitis B or Hepatitis C, Tuberculosis, COVID-19 at screening.
  16. Positive urine drug test or positive breath alcohol test at screening or at admission to the clinical unit.
  17. Any medication (including St John's Wort) within 14 days before administration, or within 5 times the elimination half-life of that drug, whichever is the longest.
  18. Treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) prior to dosing.
  19. Unable to refrain from consumption of grapefruit and grapefruit juice, orange fruit & orange juice within 7 days prior to the first dose of study medication.
  20. Unwillingness to abstain from sexual intercourse with pregnant or lactating women or to use a condom and spermicide and another form of contraception (e.g., IUD, birth control pills taken by female partner, diaphragm with spermicide) if engaging in sexual intercourse with a woman who could become pregnant until discharge from the study and during 90 additional days.
  21. Subjects unlikely to co-operate in the study, and/or poor compliance anticipated by the investigator.
  22. Subject being in the exclusion period of a previous trial.
  23. Subject who could not be contacted in case of emergency.
  24. Subject refusing to give written informed consent.
  25. Subject who has received blood or plasma derivatives in the year preceding the study.
  26. Subject who has given blood within the past 3 months or have planned to give blood or sperm within the 90 days following the study.
  27. Subject who has forfeited their freedom by administrative or legal award, or who is under guardianship or under limited judicial protection.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Sekvensiell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: SAD Group 1
Random allocation to placebo or active RNV-166- 200 mg
RNV-166 will be formulated as 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Placebo capsules will be identical to RNV-166 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Eksperimentell: SAD Group 2
Random allocation to placebo or active RNV-166- 400 mg
RNV-166 will be formulated as 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Placebo capsules will be identical to RNV-166 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Eksperimentell: SAD Group 3
Random allocation to placebo or active RNV-166- 800 mg
RNV-166 will be formulated as 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Placebo capsules will be identical to RNV-166 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Eksperimentell: SAD Group 4
Random allocation to placebo or active RNV-166- 1200 mg
RNV-166 will be formulated as 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Placebo capsules will be identical to RNV-166 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Eksperimentell: SAD Group 5
Random allocation to placebo or active RNV-166- 1600 mg
RNV-166 will be formulated as 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Placebo capsules will be identical to RNV-166 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Eksperimentell: SAD Group 6
Random allocation to placebo or active RNV-166- 1600 mg (Food effect cohort)
RNV-166 will be formulated as 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Placebo capsules will be identical to RNV-166 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Eksperimentell: MAD Group 1
Random allocation to placebo or active RNV-166- 200 mg
RNV-166 will be formulated as 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Placebo capsules will be identical to RNV-166 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Eksperimentell: MAD Group 2
Random allocation to placebo or active RNV-166- 800 mg capsules
RNV-166 will be formulated as 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Placebo capsules will be identical to RNV-166 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Eksperimentell: MAD Group 3
Random allocation to placebo or active RNV-166- 1600 mg
RNV-166 will be formulated as 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort
Placebo capsules will be identical to RNV-166 200 mg capsules, participants of different cohorts will administer the appropriate number of capsules to meet the dose of the cohort

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Safety- Treatment Emergent Adverse Events
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Number and type of treatment emergent adverse events (TEAE) following RNV-166 administration will be assessed
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of clinical laboratory and changes from baseline will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Laboratory values include hematology, biochemistry, clinical chemistry, coagulation, and urinalysis
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of 12-lead ECG parameter of heart rate (number of heart beats per minute) and changes from baseline will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
ECG parameters include heart rate (number of heart beats per minute)
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of vital signs and changes from baseline with respect to body temperature (in degree Fahrenheit) will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Vital signs include body temperature (in degree Fahrenheit)
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of 12-lead ECG parameter of PR interval (milliseconds) and changes from baseline will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
ECG parameters include PR interval (milliseconds)
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of 12-lead ECG parameter of QRS duration (milliseconds) and changes from baseline will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
ECG parameters include QRS duration (milliseconds)
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of 12-lead ECG parameter of QT interval (milliseconds) and changes from baseline will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
ECG parameters include QT interval (milliseconds)
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of 12-lead ECG parameter of QTcF interval (milliseconds) and changes from baseline will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
ECG parameters include QTcF interval (milliseconds)
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of vital signs- respiratory rate (breathes per minute) and changes from baseline will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Vital signs include respiratory rate (breathes per minute)
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of vital signs- blood pressure (mmHg) and changes from baseline will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Vital signs include blood pressure (mmHg)
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Evaluations of vital signs- radial pulse (beats per minute) and changes from baseline will be assessed using descriptive statistics following RNV-166 administration
Tidsramme: Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)
Vital signs include radial pulse (beats per minute)
Day 1 through Day 7-10 (SAD) or Day 40-46 (MAD)

Sekundære resultatmål

Resultatmål
Tidsramme
Maximum plasma concentration (Cmax)
Tidsramme: SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose
SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose
Area under the plasma concentration versus time curve (AUC)
Tidsramme: SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose
SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose
Time to maximum concentration (Tmax)
Tidsramme: SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose
SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose
Terminal elimination half-life (t1/2)
Tidsramme: SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose
SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose
Apparent oral plasma clearance (CL/F)
Tidsramme: SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose
SAD: Up to Day 2, 48 hours post dose; MAD: up to Day 28, 36 hours post last dose

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Studiestol: Dr Biswajit Nag, Ph.D, Renovel Innovations

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

22. august 2024

Primær fullføring (Faktiske)

29. september 2024

Studiet fullført (Faktiske)

5. februar 2025

Datoer for studieregistrering

Først innsendt

10. februar 2026

Først innsendt som oppfylte QC-kriteriene

4. september 2026

Først lagt ut (Faktiske)

9. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

9. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • iVRS-CD-23-027

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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