A Study to Evaluate the Safety, Tolerability and PK of SK-08

Recruiting now · Phase 1 · Has a placebo group

Conditions studied: Chronic Kidney Disease(CKD)

In brief

The trial is conducted in a single-center, randomized, double-blind, placebo-controlled, dose-increasing design. To evaluate the safety, tolerability, pharmacokinetics(PK) ,and pharmacodynamics (PD) characteristics of SK-08 in healthy participants.

Key facts

Study ID

NCT07021157

Run by

Consun Pharmaceutical Group

People needed

48

Starts

2025-03-09

Expected to finish

2025-08-07

Last updated by the study team

2025-06-24

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy male and female participants aged 18 to 45 years (inclusive).
• Male participants: Body weight ≥50 kg; Female participants: Body weight ≥45 kg; Body mass index (BMI) between 19.0 and 26 kg/m².
• Participants must have no plans for conception during the trial and for 3 months after the last dose, and must voluntarily use effective contraception with no plans for sperm or egg donation .
• Capable of understanding and voluntarily providing written informed consent prior to any study-related procedures.

You may not qualify if…

• Have a specific history of allergies or have an allergic constitution；
• Have a history of chronic diseases or severe diseases in the cardiovascular, liver, kidney, biliary tract, respiratory, blood and lymphatic, endocrine, immune, mental, neuromuscular, gastrointestinal systems, etc.
• Developed acute diseases from 2 weeks before screening to before randomization ;
• Patients with previous or current hypotension or insufficient blood volume, intracranial hypertension or cerebral hemorrhage, or those with ocular diseases (such as angle-closure glaucoma), who are not suitable for inclusion after assessment by the researcher;
• Those with clinical significance hypokalemia, hyperkalemia, hypomagnesemia, hypermagnesemia, hypocalcemia, and hypercalcemia;
• Those who have used any drugs or health supplements from 2 weeks before screening to randomization ;
• Any drugs that may interact with this product have been used from 30 days before screening to randomization, such as CYP450 inhibitors or inducers ;
• Those who have undergone major surgical operations from 6 months before screening , or who plan to undergo surgery during the study period, or who have undergone surgeries as judged by the investigator to affect drug absorption, distribution, metabolism, and excretion;
• Those who have received live attenuated vaccine inoculation from 2 weeks before screening to randomization or those who need to receive live attenuated vaccine inoculation during the trial;
• Those who had a history of alcohol abuse within one year before screening；
• Those who smoked more than 5 cigarettes per day on average within 3 months before screening and before randomization, or were unable to stop using any tobacco products during the trial period;
• Those who cannot tolerate venipuncture/indwelling needles or have a history of fainting from needles or blood ;
• Other researchers determined that the subjects were not suitable to participate.

Where it is running

• The First Affiliated Hospital，Zhejiang University — Hangzhou, Zhejiang, China (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.