Safety and Pharmacokinetics of JAK/ROCK Inhibitor in Healthy Volunteers

The following clinical trial consists of two phases IA and IB. Approximately 68 volunteers who meet all the inclusion and none of the exclusion criteria are going to be enrolled into the study. Phase IA (approx. 24 male and female volunteers) is to evaluate safety and tolerability after single oral administration of the Investigational Medicinal Produkt (IMP) to healthy volunteers. Additional cohort (approx 12 healthy volunteers) is going to be included in the phase IA of the study to assess the food effect on CPL409116 compound's bioavailability after one dose of single oral IMP administration. There are to be two treatments periods for this cohort: fasted and fed. Phase IB (approx. 32 male and female volunteers) is to evaluate safety and tolerability after two weeks of oral administration of IMP to healthy volunteers.

Inclusion criteria

• Body-mass index (BMI): ≥ 18.5 kg/m² and < 29.9 kg/m²,
• Physical examination (such as observation, palpation, percussion and auscultation) without any clinically relevant abnormality,
• Clinical laboratory results in hematology or renal/hepatic test and clinical laboratory results in other tests without any clinically relevant abnormalities as assessed by Investigator,
• Non-smoker and non-user of tobacco products for at least 3 months before screening,
• Subject able to provide written informed consent after receiving information about the trial,
• Informed Consent Form signed and dated prior to Screening evaluations,
• Ability and willingness to comply with the requirements of the study protocol,
• Volunteer (or his/her partner) of childbearing potential willingness to use acceptable forms of contraception: complete abstinence from sexual intercourses or barrier method of spermicide (condom, diaphragm) or intrauterine device or hormonal contraceptive since at least screening evaluations for male volunteers and since at least 4 weeks before screening for female volunteers. Volunteers are furthermore willing to use it for 90 days (males) or 30 days (females) after examination at the end of the study.
• Negative result of the COVID-19 RT-PCR test (real-time reverse transcription polymerase chain reaction) for the qualitative detection of nucleic acid from SARS- CoV-2 before inclusion to the study.

Exclusion criteria

• Subject with known allergy, hypersensitivity, intolerance or contraindication to other drugs similar in structure or class to CPL409116 compound, or to any excipients of the formulation,
• Any known significant current or past acute or chronic disease or condition of the: circulatory, respiratory, hematopoietic, endocrine, nervous and musculoskeletal system, alimentary and urinary tracts, allergic disease, genetic or psychiatric disorder, thromboembolism in a volunteer or in members of their close family that could influence the present general health condition, at the Investigator's discretion,
• Thrombophilia or genetic predisposition to thrombophilia in a volunteer and/or previous or current thromboembolic events/ disease in a volunteer or in members of their family,
• Subject has a long QT interval analysis syndrome or is under the treatment with antiarrhythmic drugs,
• Current disease of the alimentary tract, liver or kidneys that may influence absorption, distribution and/or elimination of the studied drug, as assessed by the Investigator and documented in the medical history,
• Medical condition that requires administration of other drugs or use of any drug within the 4 weeks preceding the first IMP administration and during the entire study. Drugs commonly used with fast metabolism may be administered and is up to Investigator discretion (i.e. pain killers),
• Participation in other clinical trials, where at least one dose of study drug was administered, within 90 days preceding the screening phase,
• Blood drawn within 30 days prior to inclusion in this study (more or equal to 300 mL),
• Positive results from pregnancy test in female volunteers,
• Lactation in female volunteers,
• Hypotension or hypertension in medical history, on Screening Day or before treatment period, if Principal Investigator is to assess it as clinically relevant,
• Narcotic and alcohol addiction or abuse (more than 14 alcohol units per week: one unit = 150 mL wine, 360 mL beer, 45 mL 40 % spirits) (UK guidelines),
• Positive results of HBsAg, anti-HCV or anti-HIV tests,
• Positive drug screen or alcohol breath tests,
• Subjects who adhere to a special diet (e.g. low calories, vegetarian, etc.),
• The subject is considered by the Investigator to be an unsuitable candidate to participate in the study for any reason.