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85,013 comparisons from ClinicalTrials.gov. Counted 2026-11-10.

85,013 comparisons

Most participants first33,758 with no events in either group come last1,561 to 1,580 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
Palbociclib Plus Endocrine Therapy (Arm A) vs Endocrine Therapy Alone (Arm B): deaths from any cause99 of 2,841

76 of 2,902

0.9 points

-0.0 to 1.8

5,743NCT02513394

PALbociclib CoLlaborative Adjuvant Study

Palbociclib Plus Endocrine Therapy (Arm A) vs Endocrine Therapy Alone (Arm B): serious adverse events369 of 2,841

229 of 2,902

5.1 points

3.5 to 6.7

5,743NCT02513394

PALbociclib CoLlaborative Adjuvant Study

Telmisartan (TRANSCEND) vs Placebo (TRANSCEND): TRANSCEND. New Onset of Atrial Fibrillation181 of 2,851

182 of 2,870

0.0 points

-1.3 to 1.3

5,721NCT00153101

Effectiveness and Safety of Ramipril Alone Compared With Telmisartan Alone and in Combination With Ramipril in Patients at High Risk for Cardiovascular Events. Patients Intolerant to Ramipril Were Entered in TRANSCEND, Telmisartan Compared to Placebo.

Group 1: rLP2086 vs Group 2: HAV/Saline/HAV: serious adverse events59 of 3,796

48 of 1,908

-1.0 points

-1.8 to -0.2

5,704NCT01352793

A Global Phase 3 Safety Study of 120 mcg rLP2086 Vaccine in Adolescents and Young Adults Aged 10 to 25 Years

QIVc vs Comparator: deaths from any cause1 of 2,856

2 of 2,841

-0.0 points

-0.2 to 0.1

5,697NCT03932682

Efficacy Study With QIVc in Pediatric Subjects

QIVc vs Comparator: serious adverse events64 of 2,856

84 of 2,841

-0.7 points

-1.6 to 0.1

5,697NCT03932682

Efficacy Study With QIVc in Pediatric Subjects

All TNFi Initiators Combination vs All TNFI Initiators Monotherapy: Number of Participants With mACR20 at 6 Months for TNFi Monotherapy vs TNFi Combination With MTX1,224 of 4,013

394 of 1,683

7.1 points

4.6 to 9.5

5,696NCT05576051

To Estimate the Efficacy of Treatment With TNFi as Monotherapy or Combination Therapy With MTX and Compare and Contrast Efficacy With Tofacitinib as Monotherapy and Combination Therapy in a Real World Setting.

Adherence Intervention vs Usual Care: deaths from any cause28 of 2,879

24 of 2,808

0.1 points

-0.4 to 0.6

5,687NCT03748420

Medication Adherence Clinical Decision Support

Adherence Intervention vs Usual Care: serious adverse events559 of 2,879

557 of 2,808

-0.4 points

-2.5 to 1.6

5,687NCT03748420

Medication Adherence Clinical Decision Support

Finerenone vs Placebo: All-cause Mortality219 of 2,833

244 of 2,841

-0.9 points

-2.3 to 0.6

5,674NCT02540993

Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and Diabetic Kidney Disease

Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Onset of Kidney Failure, a Sustained Decrease of eGFR ≥40% From Baseline Over at Least 4 Weeks, or Renal Death504 of 2,833

600 of 2,841

-3.3 points

-5.4 to -1.3

5,674NCT02540993

Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and Diabetic Kidney Disease

Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Cardiovascular Death, Non-fatal Myocardial Infarction, Non-fatal Stroke, or Hospitalization for Heart Failure367 of 2,833

420 of 2,841

-1.8 points

-3.6 to -0.0

5,674NCT02540993

Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and Diabetic Kidney Disease

Finerenone vs Placebo: All-cause Hospitalization1,263 of 2,833

1,321 of 2,841

-1.9 points

-4.5 to 0.7

5,674NCT02540993

Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and Diabetic Kidney Disease

Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Onset of Kidney Failure, a Sustained Decrease in eGFR of ≥57% From Baseline Over at Least 4 Weeks, or Renal Death252 of 2,833

326 of 2,841

-2.6 points

-4.2 to -1.0

5,674NCT02540993

Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and Diabetic Kidney Disease

Finerenone vs Placebo: deaths from any cause222 of 2,833

250 of 2,841

-1.0 points

-2.4 to 0.5

5,674NCT02540993

Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and Diabetic Kidney Disease

LCZ696 (Sacubitril/Valsartan) vs Ramipril: Number of Participants With a Confirmed Composite of HF Hospitalization or Outpatient HF201 of 2,830

237 of 2,831

-1.3 points

-2.7 to 0.1

5,661NCT02924727

Prospective ARNI vs ACE Inhibitor Trial to DetermIne Superiority in Reducing Heart Failure Events After MI

LCZ696 (Sacubitril/Valsartan) vs Ramipril: Number of Participants With a Confirmed Composite of CV Death or HF Hospitalization308 of 2,830

335 of 2,831

-0.9 points

-2.6 to 0.7

5,661NCT02924727

Prospective ARNI vs ACE Inhibitor Trial to DetermIne Superiority in Reducing Heart Failure Events After MI

LCZ696 (Sacubitril/Valsartan) vs Ramipril: All-cause Mortality for Full Analysis Set (FAS)213 of 2,830

242 of 2,831

-1.0 points

-2.4 to 0.4

5,661NCT02924727

Prospective ARNI vs ACE Inhibitor Trial to DetermIne Superiority in Reducing Heart Failure Events After MI

LCZ696 (Sacubitril/Valsartan) vs Ramipril: Number of Participants With a Confirmed Composite of CV Death, Non-fatal Spontaneous Myocardial Infarction or Non-fatal Stroke315 of 2,830

349 of 2,831

-1.2 points

-2.9 to 0.5

5,661NCT02924727

Prospective ARNI vs ACE Inhibitor Trial to DetermIne Superiority in Reducing Heart Failure Events After MI

Finerenone vs Placebo: serious adverse events902 of 2,827

971 of 2,831

-2.4 points

-4.8 to 0.1

5,658NCT02540993

Efficacy and Safety of Finerenone in Subjects With Type 2 Diabetes Mellitus and Diabetic Kidney Disease

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Words from a trial's title, conditions or interventions, its outcome or its groups, or an NCT number.

An outcome counted in participants, the serious adverse events, or the deaths from any cause.

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Response

The first 2 of this page's 20 results. GET /api/comparisons/v1?page=79

{
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      {
        "id": "NCT02513394-deaths",
        "title": "Palbociclib Plus Endocrine Therapy (Arm A) vs Endocrine Therapy Alone (Arm B): deaths from any cause",
        "summary": "99 of 2841 against 76 of 2902; risk difference 0.9 points, 95% interval -0.0 to 1.8; NCT02513394, PALbociclib CoLlaborative Adjuvant Study",
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        "trial_title": "PALbociclib CoLlaborative Adjuvant Study"
      },
      {
        "id": "NCT02513394-sae",
        "title": "Palbociclib Plus Endocrine Therapy (Arm A) vs Endocrine Therapy Alone (Arm B): serious adverse events",
        "summary": "369 of 2841 against 229 of 2902; risk difference 5.1 points, 95% interval 3.5 to 6.7; NCT02513394, PALbociclib CoLlaborative Adjuvant Study",
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trial-comparisons-2026-03-23-0.1.0Next page

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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