MedPath

Clinical Study for the Evaluation of Safety and Tolerability of NCP112 Eye Drops

Phase 1
Recruiting
Conditions
Xerophthalmia
Interventions
Drug: NCP112 Placebo
Registration Number
NCT06263998
Lead Sponsor
Huons Co., Ltd.
Brief Summary

The objective is to evaluate the safety, local tolerability, and pharmacokinetics of NCP112 eye drops through single and multiple dose-escalation ocular administrations in healthy adults.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  1. Healthy adult subjects aged 19 to 50 years at the time of screening (Visit 1).

  2. Subjects with a body weight of 50.0 kg or more, and a body mass index (BMI) between 18.0 kg/m² and 30.0 kg/m² at the time of screening (Visit 1).

    ※ Body Mass Index (BMI, kg/m²) = Weight (kg) / [Height (m)]²

  3. Subjects who have received sufficient explanation about the clinical trial, fully understand it, and have voluntarily decided to participate and signed the written informed consent.

  4. Subjects deemed suitable as participants for this clinical trial based on the investigators judgment after physical examination, clinical laboratory tests, and medical history obtained during screening (Visit 1).

Exclusion Criteria
  1. Subjects with clinically significant diseases or history of diseases related to the liver, kidneys, cardiovascular system, gastrointestinal system, respiratory system, musculoskeletal system, endocrine system, neuropsychiatric system (such as epilepsy, mood disorders, obsessive-compulsive disorder), hematologic/oncologic system, or urinary system (chronic or recurrent urinary tract infections).

  2. Subjects with hepatitis B or C.

  3. Subjects meeting any of the following criteria based on ophthalmologic history or examination during screening (Visit 1):

    • Corrected visual acuity of 20/40 or less.
    • Intraocular pressure exceeding 21 mmHg in either eye.
    • History of lacrimal drainage system disease or abnormal tear drainage.
    • History or suspicion of conditions affecting visual organs such as keratitis, iritis, uveitis, retinitis, dry eye syndrome, strabismus, glaucoma, etc.
    • Experience of adverse effects from contact lens use, or contact lens use within one month prior to the anticipated first dose, or inability to abstain from contact lens use during the clinical trial.
    • Ophthalmologic surgery (intraocular surgery) or laser vision correction surgery (such as LASIK) within 12 months prior to the anticipated first dose.
    • Silicone punctal occlusion or punctal cauterization within 3 months prior to the anticipated first dose (collagen punctal occlusion within 1 month).
    • Any other abnormal findings from ophthalmologic examination.
  4. Subjects with a history of hypersensitivity to the active ingredients or excipients of the investigational drug, or to drugs in the same class as the active ingredients.

  5. Subjects who have taken any medications related to dry eye syndrome (e.g., artificial tears, anti-inflammatory agents like cyclosporine, hyaluronic acid preparations, tetracycline preparations) or drugs that could induce dry eye syndrome or affect the outcome of this clinical trial (e.g., oral contraceptives, antihistamines, sedatives, oral aspirin, corticosteroids) within one month prior to the anticipated first dose.

  6. Subjects who have taken any prescription drugs, eye drops other than those for dry eye, oriental medicine, or any other health supplements, including liver function supplements or vitamins within 2 weeks of the expected first dosing date, or any over-the-counter drugs within 1 week (unless other conditions are deemed appropriate by the investigator).

  7. Subjects who have taken drug metabolism inducers or inhibitors, such as barbiturates, within one month prior to the expected first dosing date

  8. Subjects with a history of drug abuse or a positive result on a urine drug test at screening (Visit 1).

  9. Subjects unable to restrict grapefruit or grapefruit-containing food consumption from 7 days prior to the anticipated first dose through the duration of the clinical trial.

  10. Subjects with systolic blood pressure of 90 mmHg or less, or 140 mmHg or more, or diastolic blood pressure of 50 mmHg or less, or 90 mmHg or more after sitting for at least 3 minutes without sudden postural changes during screening (Visit 1).

  11. Subjects with a history of alcohol abuse, or who have consumed alcohol regularly (more than 21 units/week, 1 unit = 10 g = 12.5 mL of pure alcohol) within one month prior to the anticipated first dose, or are unable to abstain from alcohol during the clinical trial.

  12. Subjects who regularly consume caffeine (e.g., coffee or green tea more than 5 units/day) or are unable to abstain from caffeine-containing foods from 24 hours prior to hospitalization through the duration of the clinical trial.

  13. Subjects who have regularly smoked (including e-cigarettes, more than 10 cigarettes/day) within one month prior to the anticipated first dose, or are unable to abstain from smoking during the clinical trial.

  14. Subjects who test positive on a breath alcohol test at screening (Visit 1).

  15. Subjects who have participated in another clinical trial and received an investigational drug within 6 months prior to the anticipated first dose.

  16. Subjects who have donated whole blood within 2 months, or component blood within 1 month, or received a blood transfusion within 1 month prior to the anticipated first dose, or who plan to donate or receive blood during the clinical trial.

  17. Subjects who have received a vaccine within 14 days prior to the anticipated first dose or are expected to receive a vaccine during the trial period.

  18. Female participants who test positive on a pregnancy test (urine hCG) conducted before the start of investigational drug administration, are pregnant, or are breastfeeding, except for those who have undergone surgical sterilization (Bilateral tubal ligation, Bilateral oophorectomy, or Hysterectomy).

  19. Subjects who, during the entire clinical trial period and for at least 90 days after the last dose of the investigational drug, cannot or do not agree to use medically acceptable double contraception methods, or whose partner cannot or does not agree to use medically acceptable contraception, or who do not agree to refrain from donating sperm during this period.

    ※ Medically acceptable contraception methods include:

    • Use of an intrauterine device (IUD) with a documented failure rate by the partner.
    • Double contraception (use of barrier methods by both male and female partners).
    • Surgical sterilization of the subject or partner (vasectomy, tubal ligation, hysterectomy).
  20. Subjects deemed unsuitable for participation by the investigator for other reasons (e.g., non-compliance with instructions).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Single Ascending dose NCP112 Dose ANCP112NCP112 is administered once at a specified time in Day 1
Single Ascending dose NCP112 Dose A, PlaceboNCP112 PlaceboNCP112 Placebo is administered once at a specified time in Day 1
Single Ascending dose NCP112 Dose BNCP112NCP112 is administered once at a specified time in Day 1
Single Ascending dose NCP112 Dose B, PlaceboNCP112 PlaceboNCP112 Placebo is administered once at a specified time in Day 1
Single Ascending dose NCP112 Dose CNCP112NCP112 is administered once at a specified time in Day 1
Single Ascending dose NCP112 Dose C, PlaceboNCP112 PlaceboNCP112 Placebo is administered once at a specified time in Day 1
Multiple Ascending dose NCP112 Dose ANCP112NCP112 is administered twice daily. \[time frame: Day 1- Day 14\]
Multiple Ascending dose NCP112 Dose A, PlaceboNCP112 PlaceboNCP112 Placebo is administered twice daily. \[time frame: Day 1- Day 14\]
Multiple Ascending dose NCP112 Dose BNCP112NCP112 is administered twice daily.\[time frame: Day 1- Day 14\]
Multiple Ascending dose NCP112 Dose B, PlaceboNCP112 PlaceboNCP112 Placebo is administered twice daily. \[time frame: Day 1- Day 14\]
Multiple Ascending dose NCP112 Dose CNCP112NCP112 is administered twice daily.\[time frame: Day 1- Day 14\]
Multiple Ascending dose NCP112 Dose C, PlaceboNCP112 PlaceboNCP112 Placebo is administered twice daily. \[time frame: Day 1- Day 14\]
Primary Outcome Measures
NameTimeMethod
Eye irritation(Likert scale)Single dose Day -1 ~ Day 4, Multiple dose Day -1 ~ Day 22

Local safety assessment

Eye redness(Likert scale)Single dose Day -1 ~ Day 4, Multiple dose Day -1 ~ Day 22

Local safety assessment

Intraocular pressureSingle dose Day -1 ~ Day 4, Multiple dose Day -1 ~ Day 22

Opthalmic examination

History takingSingle dose Day -1 ~ Day 4, Multiple dose Day -1 ~ Day 22

Opthalmic examination

Corrected vision testSingle dose Day -1 ~ Day 4, Multiple dose Day -1 ~ Day 22

Opthalmic examination

Adverse eventsSingle dose Day -1 ~ Day 4, Multiple dose Day -1 ~ Day 22

Including subjective and objective symptoms

Vital signsSingle dose Day -1 ~ Day 4, Multiple dose Day -1 ~ Day 22

Blood pressure

Secondary Outcome Measures
NameTimeMethod
CmaxDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

AUClastDay 1~Day 4 (Blood sampling at specified times within the time frame)

Single dose - Evaluation of pharmacokinetic profile

TmaxDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

AUCinfDay 1~Day 4 (Blood sampling at specified times within the time frame)

Single dose - Evaluation of pharmacokinetic profile

t1/2Day 1~Day 4 (Blood sampling at specified times within the time frame)

Single dose - Evaluation of pharmacokinetic profile

CL/FDay 1~Day 4 (Blood sampling at specified times within the time frame)

Single dose - Evaluation of pharmacokinetic profile

Vz/FDay 1~Day 4 (Blood sampling at specified times within the time frame)

Single dose - Evaluation of pharmacokinetic profile

AUCtauDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

Cmax,ssDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

AUCtau,ssDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

Cmin,ssDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

t1/2,ssDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

CLss/FDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

Vz,ss/FDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

PTFDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

RDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

Tmax,ssDay 1~Day 22 (Blood sampling at specified times within the time frame)

Multiple dose - Evaluation of pharmacokinetic profile

Trial Locations

Locations (1)

Seoul National University Hospital

🇰🇷

Seoul, Daehak-ro, Jongno-gu, Korea, Republic of

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