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Phase 1 Completed N=30 Treatment

A Study of Silmitasertib (CX-4945) in Healthy Subject

Source: ClinicalTrials.gov NCT05817708 ↗
Enrolled (actual)
30
Serious AEs
0.0%
Results posted
Jan 2025
Primary outcomePrimary: Number of Participants With Treatment-emergent Adverse Events (TEAT) — 1; 3; 7 Participants

Summary

This is a Phase I single center, open-label, parallel design in 30 subjects to evaluate safety and tolerability of CX-4945 200mg QD, 200 mg BID and 400mg BID doses (10 subjects in each regimen) for continuously 5 days in healthy subjects for dose selection.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Treatment-emergent Adverse Events (TEAT)
1; 3; 7
SECONDARY
Evaluate Changes in Blood Chemistry.
-3.9; -2.4; 0.1
SECONDARY
Evaluate Changes in Blood Chemistry.
-3.9; -2.4; 0.1
SECONDARY
To Evaluate Changes in Blood Chemistry.
0.003; -0.071; 0.002
SECONDARY
To Evaluate Changes in Blood Chemistry.
0.003; -0.071; 0.002
SECONDARY
To Evaluate Changes in Blood Chemistry.
0.003; -0.071; 0.002
SECONDARY
To Evaluate Changes in Blood Chemistry.
0.003; -0.071; 0.002
SECONDARY
Number of Participants Evaluated as Having Abnormalities (CS or NCS) in Their ECG
7; 6; 6; 3; 4; 8

Eligibility Criteria

Inclusion Criteria

  • Healthy male and female subjects 20to 55 years of age, inclusive, at screening
  • Body mass index (BMI)within the range of 18.0 to 30.0 kg/m2, inclusive, and a minimum weight of 50.0 kg at screening
  • Subjects who are of reproductive potential agreed to remain abstinent or use (or have their partner use) an acceptable method of birth control (intrauterine device, hormonal contraception, vasectomy or condom) from screening until at least 2 weeks after the last study drug administration.
  • Physically and mentally healthy subjects as confirmed by an interview, medical history, clinical examination, and electrocardiogram;
  • Subject with acceptable hematology, biochemistry and urinalysis during screening period.
  • Subject is willing and able to comply with study procedures and sign informed consent.

Exclusion Criteria

  • Pregnant or nursing women. NOTE: Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence) prior to study entry and from screening until at least 2 weeks after the last study drug administration. Should a man father a child, or a woman become pregnant or suspect she is pregnant while participating in this study, he or she should inform the treating physician immediately.
  • Active or uncontrolled infections such asCOVID-19, HIV or with serious illnesses or medical conditions which would not permit the subject to receive study treatment.
  • Subject has received any prescription of drug within 3 days prior to study enrollment.
  • Subject has drug abuse history.
  • Any active or recurring clinically significant hepatic disease including HBV and HCV.
  • Subject has received any investigational agent within 28 days or 5 half-lives, whichever is longer, prior to the first dose of investigational product.
  • Any other medical reason as determined by the investigator.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05817708). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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