Trial · NCT04572841
Registered outcomes19
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 19 of 19
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change From Baseline to Week 12 in ESSDAI Score | Baseline (Day 1) to Week 12 | ESSDAI is validated and established outcome measurement for therapeutic efficacy in Sjögren's syndrome, evaluating disease activity mainly on extra-glandular manifestations. This score consists of 12 organ-specific domains (constitutional, lymphadenopathy, glandular, articular, cutaneous, pulmonary, renal, muscular, peripheral and central nervous system, hematological, biological), which are scored based on organ-specific items in 3 to 4 different severity grades (no, low, moderate, high; with 0=no and 3=high). These scores are summed up over all 12 domains in weighted way (severity grades are multiplied with weights ranging 1-6 depending on domain) to summarize into total score(0-123). Higher scores indicates worse outcome. Negative change from baseline indicates improvement. Baseline=Day 1 assessment value. Least squares (LS) mean is calculated using mixed models for repeated measures (MMRM). Observed values after occurrence of intercurrent events are excluded. |
| Secondary | Change From Baseline to Week 12 in European League Against Rheumatism (EULAR) Sjögren's Syndrome Patient Reported Index (ESSPRI) Score | Baseline (Day 1) to Week 12 | The ESSPRI is a validated and established outcome measurement, reported by participants, which rates the key disease manifestations: fatigue, dryness, and pain, based on a numeric scale ranging from 0 to 10, where 0 is defined as no symptoms and 10 as maximum imaginable complaints. The total score is the mean score of the 3 scales and ranges from 0 to 10. Higher scores indicates worse outcome. A negative change from baseline indicates improvement. Baseline is defined as Day 1 assessment value. LS mean is calculated using MMRM. Observed values after occurrence of intercurrent events are excluded. |
| Secondary | Change From Baseline to Week 12 in Multidimensional Fatigue Inventory (MFI) General Fatigue Subscale and Other Subscales Score | Baseline (Day 1) to Week 12 | The MFI is a validated, 20 item self-report instrument to evaluate fatigue by investigating the following subscales: general fatigue, physical fatigue, mental fatigue, reduced motivation, and reduced activity. Each subscale consists of 4 items that are scored using a scale from 1 ("yes, this is true") to 5 ("no, this is not true") on which the participants indicate how the listed statements applied to their current fatigue situation. Item scores are summed to create individual subscale score ranging from 4 to 20. A higher score indicates a higher degree of fatigue. A negative change from baseline indicates improvement. Baseline is defined as Day 1 assessment value. LS mean is calculated using ANCOVA. Observed values after occurrence of intercurrent events are excluded. |
| Secondary | Mean Plasma Concentration of SAR441344 | At end of infusion and 4 hours post-infusion on Day 1; pre-dose at Weeks 2, 4, 6, 8, 10, and at Week 12 | Blood samples were collected at the specified timepoints for the measurement of plasma concentrations of SAR441344. |
| Secondary | Median Plasma Concentration of SAR441344 | At end of infusion and 4 hours post-infusion on Day 1; pre-dose at Weeks 2, 4, 6, 8, 10, and at Week 12 | Blood samples were collected at the specified timepoints for the measurement of plasma concentrations of SAR441344. |
| Secondary | Maximum Plasma Concentration (Cmax) of SAR441344 | After the last SC dose on Week 10 up to 336 hours post-dose | Blood samples were collected at the specified timepoints for the measurement of plasma concentrations of SAR441344. Cmax was assessed by a Bayesian approach using the population PK model. |
| Secondary | Time to Maximum Plasma Concentration (Tmax) of SAR441344 | After the last SC dose on Week 10 up to 336 hours post-dose | Blood samples were collected at the specified timepoints for the measurement of plasma concentrations of SAR441344. tmax was assessed by a Bayesian approach using the population PK model. |
| Secondary | Area Under the Curve Over the Dosing Interval (AUC0-tau) of SAR441344 | After the last SC dose on Week 10 up to 336 hours post-dose | Blood samples were collected at the specified timepoints for the measurement of plasma concentrations of SAR441344. AUC0-tau was assessed by a Bayesian approach using the population PK model. |
| Secondary | Terminal Half-life (t1/2z) of SAR441344 | Week 10 to Week 12 | Blood samples were collected at the specified timepoints for the measurement of plasma concentrations of SAR441344. t1/2z was assessed by a Bayesian approach using the population PK model. |
| Secondary | Number of Participants With Treatment-emergent Adverse Events (TEAEs), Treatment-emergent Serious Adverse Events (TESAEs), and Adverse Events of Special Interest (AESI) | From first dose of IMP (Day 1) up to end of follow-up period (Week 24) | An adverse event (AE) was any untoward medical occurrence in a participant or clinical study participant, temporally associated with the use of IMP, whether or not considered related to the IMP. TEAEs: AEs that occurred, worsened, or became serious during the TEAE period (time from the first IMP administration up to Week 24). Serious adverse events (SAE): Any untoward medical occurrence that at any dose: resulted in death, was life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent disability/incapacity, or was a congenital anomaly/birth defect. An AESI: an AE (serious or nonserious) of scientific and medical concern specific to the Sponsor's product or program, for which ongoing monitoring and immediate notification by the Investigator to the Sponsor was required. |
| Secondary | Number of Participants With Treatment Discontinuation and Withdrawals Due to TEAEs | From first dose of IMP (Day 1) up to end of follow-up period (Week 24) | An AE was any untoward medical occurrence in a participant or clinical study participant, temporally associated with the use of IMP, whether or not considered related to the IMP. TEAEs were AEs that occurred, worsened, or became serious during the TEAE period (time from the first IMP administration up to Week 24). |
| Secondary | Number of Participants With Increase in Pain Intensity Compared to Pre-dose Pain Intensity at Injection Site by Verbal Descriptor Scale (VDS) | Pre-dose (within 24 hours prior IMP dosing), post-dose (up to 15 minutes after dosing) and 2 hours post-dose at Weeks 2, 4, 6, 8 and 10 | For the measurement of local tolerability, participants had a self-evaluation using a VDS before IMP administration, after completion of the IMP administration, and 2 hours post-administration. The participants were asked to report sensations at the injection site and rated the pain severity as following grading: 0= no pain; 1= mild pain; 2= moderate pain, 3= severe pain, 4= very severe. A positive change in VDS score indicated a higher pain severity compared to the pre-dose pain. The numerical change provides the number of grades the pain got worse (positive change) or improved (negative change). Total number of participants with pain intensity increase (change in VDS score of greater than or equal to 1) compared to pre-dose pain intensity are reported. |
| Secondary | Number of Participants With AEs Related to Local Tolerability Findings | Baseline (Day 1) to Week 10 | An AE was any untoward medical occurrence in a participant or clinical study participant, temporally associated with the use of IMP, whether or not considered related to the IMP. Local tolerability at injection site was assessed following IMP injection and findings at the site of injection such as injection site erythema, injection site reaction, and injection site pain were recorded. |
| Secondary | Number of Participants With Potentially Clinically Significant Abnormalities (PCSA) in Vital Signs | Baseline (Day 1) to Week 24 | PCSA values were defined as abnormal values considered medically important by the Sponsor, according to predefined criteria/thresholds based on literature reviews and defined by the Sponsor. Criteria for PCSA: Sitting systolic blood pressure (SSBP) less than or equal to (≤)95 millimeters of mercury (mmHg) and decrease from baseline ≥20 mmHg; ≥160 mmHg and increase from baseline ≥20 mmHg; Sitting diastolic blood pressure (SDBP) ≤45 mmHg and decrease from baseline ≥10 mmHg, ≥110 mmHg and increase from baseline ≥10 mmHg; Sitting heart rate (HR) ≤50 beats per minute (bpm) and decrease from baseline ≥20 bpm, ≥120 bpm and increase from baseline ≥20 bpm; Weight ≥5% decrease from baseline, ≥5% increase from baseline. |
| Secondary | Number of Participants With PCSA in Electrocardiogram | Baseline (Day 1) to Week 24 | PCSA values were defined as abnormal values considered medically important by the Sponsor, according to predefined criteria/thresholds based on literature reviews and defined by the Sponsor. Criteria for PCSA: HR \<50 bpm, \<40 bpm, \>90 bpm, \>90 bpm and increase from baseline ≥20 bpm, \>100 bpm; PR interval, aggregate \>200 milliseconds (msec), \>200 msec and increase from baseline ≥25%, \>220 msec, \>220 msec and increase from baseline ≥25%, \>240 msec, \>240 msec and increase from baseline ≥25%; QRS duration, aggregate \>110 msec, \>110 msec and increase from baseline ≥25%, \>120 msec, \>120 msec and increase from baseline ≥25%; QT interval, aggregate \>500 msec; corrected QT (QTc) correction method unspecified \>450 msec, \>480 msec, increase from baseline \[30-60\] msec, increase from baseline \>60 msec. |
| Secondary | Number of Participants With PCSA in Hematology Parameters | Baseline (Day 1) to Week 24 | PCSA values were defined as abnormal values considered medically important by the Sponsor, according to predefined criteria/thresholds based on literature reviews and defined by the Sponsor. Criteria for PCSA: Hemoglobin (Hb) ≤115 grams per liter (g/L) (Male \[M\]) or ≤95 g/L (Female \[F\]), ≥185 g/L (M) or ≥165 g/L (F), decrease from baseline ≥20 g/L; Hematocrit ≤0.37 volume per volume (v/v) (M) or ≤0.32 v/v (F), ≥0.55 v/v (M) or ≥0.5 v/v (F); Erythrocytes (red blood cells \[RBC\]) ≥6 x 10\^12 per liter (/L); Platelets \<100 x 10\^9/L, ≥700 x 10\^9/L; Leukocytes (white blood cells \[WBC\]) \<3 x 10\^9/L (Non-Black\[NB\]) or \<2 x 10\^9/L (Black\[B\]), ≥16 x 10\^9/L; Neutrophils \<1.5 x 10\^9/L (NB) or \<1 x 10\^9/L (B); Lymphocytes \>4 x 10\^9/L, \<0.5 x 10\^9L; Monocytes \>0.7 x 10\^9/L; Basophils \>0.1 x 10\^9/L; Eosinophils \>0.5 x 10\^9/L or \>upper limit of normal(ULN) (if ULN ≥0.5 x 10\^9/L). |
| Secondary | Number of Participants With PCSA in Clinical Chemistry Parameters | Baseline (Day 1) to Week 24 | PCSA values:abnormal values considered medically important by Sponsor, according to predefined criteria/thresholds based on literature reviews and defined by Sponsor.Criteria for PCSA:Sodium≤129 millimoles per liter(mmol/L),≥160 mmol/L;Potassium\<3 mmol/L,≥5.5 mmol/L;Glucose≤3.9 mmol/L and \<lower limit of normal(LLN),≥11.1 mmol/L(unfasted);≥7 mmol/L(fasted); Creatine kinase(CK)\>3 ULN,\>10 ULN;Creatinine≥150 micromoles/L(adults),≥30% change from baseline,≥100% change from baseline;Creatinine clearance(CG)≥60-\<90 milliliters per minute(mL/min)(mild decrease in glomerular filtration rate\[GFR\]),≥30-\<60 mL/min(moderate decrease in GFR),≥15-\<30 mL/min(severe decrease in GFR),\<15 mL/min(end stage renal disease),Urea nitrogen≥17 mmol/L;Alkaline phosphatase(ALP)\>1.5 ULN;Alanine aminotransferase(ALT)\>3 ULN; ALT\>3 ULN and bilirubin\>2 ULN;Aspartate aminotransferase(AST)\>3 ULN;Direct bilirubin\>35% bilirubin and bilirubin\>1.5 ULN;Total bilirubin\>1.5 ULN,\>2 ULN. |
| Secondary | Number of Participants With PCSA in Urinalysis Parameters | Baseline (Day 1) to Week 24 | PCSA values were defined as abnormal values considered medically important by the Sponsor, according to predefined criteria/thresholds based on literature reviews and defined by the Sponsor. Criteria for PCSA: Potential of hydrogen (pH) ≤4.6 or ≥8. |
| Secondary | Number of Participants With Anti-drug Antibodies (ADA) to SAR441344 | Baseline, Week 4, Week 8, Week 12, and Week 24 | Serum samples were collected at the specified timepoints for the assessment of ADAs to SAR441344. Number of participants with treatment-emergent ADA defined as at least 1 treatment-induced/boosted ADA during the treatment-emergent period, i.e. from the time of the IMP administration up to the end of study visit are reported. Number of participants with positive ADA are reported. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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