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Phase 1 Completed N=69 Basic Science

Effects Of CP-690,550 (Tasocitinib) On Cholesterol Metabolism In Patients With Active Rheumatoid Arthritis

Source: ClinicalTrials.gov NCT01262118 ↗
Enrolled (actual)
69
Serious AEs
0.0%
Results posted
Jan 2013
Primary outcomePrimary: High-density Lipoprotein Cholesterol (HDL-C) Concentration at Baseline — 54.30; 63.43 milligram per deciliter (mg/dL)

Summary

The purpose of study is to explore the effect of CP-690,550 (tasocitinib) on cholesterol metabolism in patients with active rheumatoid arthritis (RA).

Outcome Measures

OutcomeResultp-value
PRIMARY
High-density Lipoprotein Cholesterol (HDL-C) Concentration at Baseline
54.30; 63.43
PRIMARY
High-density Lipoprotein Cholesterol (HDL-C) Concentration at Week 6
62.34
PRIMARY
Cholesterol Ester Production Rate at Baseline
1.09; 1.11
PRIMARY
Cholesterol Ester Production Rate at Week 6
1.12
SECONDARY
Low-density Lipoprotein Cholesterol (LDL-C) and Total Cholesterol Concentration
124.61; 144.88; 193.79; 221.57; 142.68; NA
SECONDARY
Cholesterol Ester Fractional Catabolic Rate
2.43; 2.17; 2.23; NA
SECONDARY
Low-density Lipoprotein Associated With Apolipoprotein B (LDL-apoB) Production Rate
0.49; 0.50; 0.52; NA
SECONDARY
Low-density Lipoprotein Associated With Apolipoprotein B (LDL-apoB) Fractional Catabolic Rate
1.61; 1.50; 1.57; NA
SECONDARY
High-density Lipoprotein Associated With Apolipoprotein A1 (HDL-apoA1) Production Rate
0.57; 0.59; 0.65; NA
SECONDARY
High-density Lipoprotein Associated With Apolipoprotein A1 (HDL-apoA1) Fractional Catabolic Rate
1.08; 1.02; 1.11; NA
SECONDARY
Cholesterol Efflux Rate
4.02; 4.35; 4.04; NA

Eligibility Criteria

Inclusion Criteria

  • Males or females, 18 years of age or older with active rheumatoid arthritis; Or male and female healthy volunteers 18 years of age and older

Exclusion Criteria

  • Pregnant or lactating women
  • Clinically significant systemic disease (other than RA for RA arm)
  • Use of lipid-regulating agents
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01262118). 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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