Trial · NCT02250443
Results by group68
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 68
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Participants With Adverse Events as a Measure of Safety and Tolerability | BYM338 | Death | 0 | Participants | |
| Number of Participants With Adverse Events as a Measure of Safety and Tolerability | BYM338 | Serious adverse events (SAE) | 2 | Participants | |
| Number of Participants With Adverse Events as a Measure of Safety and Tolerability | BYM338 | Adverse Events (AE) | 10 | Participants | |
| Changes From Baseline in Lean Body Mass (LBM) by Dual-Energy X-ray Absorptiometery (DXA) | BYM338 | Day 1 | 0 | Standard Deviation 0 | Percentage Change in LBM |
| Changes From Baseline in Lean Body Mass (LBM) by Dual-Energy X-ray Absorptiometery (DXA) | BYM338 | Day 57 | 4.292 | Standard Deviation 2.7480 | Percentage Change in LBM |
| Changes From Baseline in Lean Body Mass (LBM) by Dual-Energy X-ray Absorptiometery (DXA) | BYM338 | Day 113 | 5.552 | Standard Deviation 3.6066 | Percentage Change in LBM |
| Changes From Baseline in Lean Body Mass (LBM) by Dual-Energy X-ray Absorptiometery (DXA) | BYM338 | Day 169 | 7.463 | Standard Deviation 4.5687 | Percentage Change in LBM |
| Changes From Baseline in Lean Body Mass (LBM) by Dual-Energy X-ray Absorptiometery (DXA) | BYM338 | Day 365 | 6.919 | Standard Deviation 2.9669 | Percentage Change in LBM |
| Changes From Baseline in Lean Body Mass (LBM) by Dual-Energy X-ray Absorptiometery (DXA) | BYM338 | Day 533 | 6.885 | Standard Deviation 3.7894 | Percentage Change in LBM |
| Changes From Baseline in Lean Body Mass (LBM) by Dual-Energy X-ray Absorptiometery (DXA) | BYM338 | Day 729 | 0.727 | Standard Deviation NA | Percentage Change in LBM |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 29 (n=10) | 13.4 | Standard Deviation 5.01 | ng/mL |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 85 (n=10) | 24.1 | Standard Deviation 13.1 | ng/mL |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 169 (n=10) | 26.3 | Standard Deviation 15.9 | ng/mL |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 253 (n=9) | 28.8 | Standard Deviation 12.1 | ng/mL |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 337 (n=10) | 24.4 | Standard Deviation 14.6 | ng/mL |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 421 (n=9) | 24.5 | Standard Deviation 11.5 | ng/mL |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 505 (n=8) | 28.3 | Standard Deviation 10.6 | ng/mL |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 589 (n=6) | 39.8 | Standard Deviation 30.2 | ng/mL |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 673 (n=2) | 20.5 | Standard Deviation 1.98 | ng/mL |
| Pharmacokinetics (PK) Parameter of Cmin From Multiple i.v. Dosing | BYM338 | Day 757 (n=1) | 20.3 | Standard Deviation NA | ng/mL |
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.
For software
Read this list from software.
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GET https://conductscience.org/api/trials/v1/NCT02250443/results