Summary of findings for the main comparison. PRO 140 compared to placebo for treatment of people with HIV infection.
PRO 140 compared to placebo for treatment of people with HIV infection | ||||||
Patient or population: patients being treated for HIV infection Intervention: PRO 140 Comparison: placebo | ||||||
Outcomes | Illustrative comparative risks* (95% CI) | Relative effect (95% CI) | No of Participants (studies) | Quality of the evidence (GRADE) | Comments | |
Assumed risk | Corresponding risk | |||||
Placebo | PRO 140 | |||||
Antiviral response: 0.5 mg/kg | Study population | OR 3.00 (0.11 to 83.36) | 19 (1 study) | ⊕⊝⊝⊝ very low1,2 | ||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Moderate | ||||||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Antiviral response: 2 mg/kg | Study population | OR 27.44 (1.25 to 601.57) | 19 (1 study) | ⊕⊝⊝⊝ very low1,2 | ||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Moderate | ||||||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Antiviral response: 5 mg/kg | Study population | OR 439.09 (25.73 to 7493.14) | 40 (2 studies) | ⊕⊝⊝⊝ very low1,2 | ||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Moderate | ||||||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Antiviral response: 10 mg/kg | Study population | OR 145.67 (5.3 to 4004.91) | 21 (1 study) | ⊕⊝⊝⊝ very low1,2 | ||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Moderate | ||||||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Antiviral response: 162 mg weekly | Study population | OR 24.82 (1.17 to 527.12) | 21 (1 study) | ⊕⊝⊝⊝ very low1,2 | ||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Moderate | ||||||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Antiviral response: 324 mg weekly | Study population | OR 147.00 (5.35 to 4037.48) | 21 (1 study) | ⊕⊝⊝⊝ very low1,2 | ||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Moderate | ||||||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Antiviral response: 324 mg biweekly | Study population | OR 57.00 (2.59 to 1253.22) | 22 (1 study) | ⊕⊝⊝⊝ very low1,2 | ||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
Moderate | ||||||
0 per 1000 | 0 per 1000 (0 to 0) | |||||
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). CI: Confidence interval; OR: Odds ratio; | ||||||
GRADE Working Group grades of evidence High quality: Further research is very unlikely to change our confidence in the estimate of effect. Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low quality: We are very uncertain about the estimate. |
1 Randomization: method not specified; Allocation concealment: unclear; Blinding: method not specified. 2 Total number of events is less than 300.