Primary-outcome results across pivotal trials
Per-arm reported values from Phase 2/3 and Phase 3 trials with results posted to ClinicalTrials.gov.
| Trial | Indication | Primary endpoint | Arm | Value |
|---|---|---|---|---|
| NCT02008227 OAK | — | OS: SP-ITT Baseline until death due to any cause (up to approximately 2.87 years) | Atezolizumab | 13.3 Months |
| Docetaxel | 9.8 Months | |||
| NCT02008227 OAK | — | OS: TC1/2/3 or IC1/2/3 Subgroup of PP Baseline until death due to any cause (up to approximately 2.25 years) | Atezolizumab | 15.7 Months |
| Docetaxel | 10.3 Months | |||
| NCT02008227 OAK | — | OS: TC1/2/3 Or IC1/2/3 Subgroup of SP Baseline until death from any cause (approximately 2.87 years) | Atezolizumab | 14.3 Months |
| Docetaxel | 10.8 Months | |||
| NCT02008227 OAK | — | OS: TC2/3 or IC2/3 Subgroup of SP Baseline until death due to any cause (up to approximately 2.87 years) | Atezolizumab | 16.6 Months |
| Docetaxel | 11.4 Months | |||
| NCT02008227 OAK | — | OS: TC3 or IC3 Subgroup of SP Baseline until death due to any cause (up to approximately 2.87 years) | Atezolizumab | 20.5 Months |
| Docetaxel | 9.7 Months | |||
| NCT02008227 OAK | — | Overall Survival (OS): PP-ITT Baseline until death due to any cause (up to approximately 2.25 years) | Atezolizumab | 13.8 Months |
| Docetaxel | 9.6 Months | |||
| NCT02008227 OAK | — | Percentage of Participants Who Died: PP-ITT Baseline until death due to any cause (up to approximately 2.25 years) | Atezolizumab | 63.8 Percentage of Participants |
| Docetaxel | 70.1 Percentage of Participants | |||
| NCT02008227 OAK | — | Percentage of Participants Who Died: Tumor Cells (TC)1/2/3 or Tumor-Infiltrating Immune Cells (IC)1/2/3 Subgroup of PP Baseline until death due to any cause (up to approximately 2.25 years) | Atezolizumab | 62.7 Percentage of Participants |
| Docetaxel | 67.1 Percentage of Participants | |||
| NCT02302807 | Urinary Bladder Neoplasms | Overall Survival (OS) Between randomization and death due to any cause, up to approximately 25 months after first participant enrolled | Atezolizumab | 8.6 Months |
| Chemotherapy (Vinflunine, Paclitaxel, or Docetaxel) | 8.0 Months | |||
| IC1/2/3 Atezolizumab | 8.9 Months | |||
| IC1/2/3 Chemotherapy | 8.2 Months | |||
| IC2/3 Atezolizumab | 11.1 Months | |||
| IC2/3 Chemotherapy | 10.6 Months | |||
| NCT02366143 IMpower150 | Carcinoma, Non-Small-Cell Lung | Overall Survival (OS) in Arm A Versus Arm C in ITT-WT Population Baseline until death (up approximately 53 months) | Arm A (Atezolizumab+Paclitaxel+Carboplatin) | 19.0 Months |
| Arm C (Bevacizumab+Paclitaxel+Carboplatin) | 14.7 Months | |||
| NCT02366143 IMpower150 | Carcinoma, Non-Small-Cell Lung | Overall Survival (OS) in Arm B Versus Arm C in ITT-WT Population Baseline until death until data cut-off on 22 January 2018 (up to approximately 34 months) | Arm B (Atezolizumab+Bevacizumab+Paclitaxel + Carboplatin) | 19.2 Months |
| Arm C (Bevacizumab+Paclitaxel+Carboplatin) | 14.7 Months | |||
| NCT02366143 IMpower150 | Carcinoma, Non-Small-Cell Lung | Progression Free Survival (PFS), as Determined by the Investigator in Arm B Versus Arm C in the Teff-high WT Population and ITT-WT Population Baseline until disease progression or death, whichever occurs first until data cut-off on 15 September 2017 (up to approximately 29 months) | Arm B (Atezolizumab+Bevacizumab+Paclitaxel + Carboplatin) | 8.3 Months |
| Arm B (Atezolizumab+Bevacizumab+Paclitaxel + Carboplatin) | 11.3 Months | |||
| Arm C (Bevacizumab+Paclitaxel+Carboplatin) | 6.8 Months | |||
| Arm C (Bevacizumab+Paclitaxel+Carboplatin) | 6.8 Months | |||
| NCT02367781 IMpower130 | Carcinoma | Overall Survival (OS) in the ITT-WT Population Up to approximately 35 months after first patient enrolled | Arm A (Atezolizumab+Nab-Paclitaxel+Carboplatin) | 18.6 Months |
| Arm B (Nab-Paclitaxel+Carboplatin) | 13.9 Months | |||
| NCT02367781 IMpower130 | Carcinoma | Progression-Free Survival (PFS) as Determined by the Investigator Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) in the ITT-WT Population Up to approximately 35 months after first patient enrolled | Arm A (Atezolizumab+Nab-Paclitaxel+Carboplatin) | 7.0 Months |
| Arm B (Nab-Paclitaxel+Carboplatin) | 5.5 Months | |||
| NCT02367794 | — | Overall Survival (OS) in the ITT Population Up to approximately 39 months after first participant enrolled | Arm A: Atezolizumab + Paclitaxel + Carboplatin | 12.6 Months |
| Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin | 14.2 Months | |||
| Arm C: Nab-Paclitaxel + Carboplatin | 13.5 Months | |||
| NCT02367794 | — | Progression Free Survival (PFS) as Determined by the Investigator Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) in the Intent-to-Treat (ITT) Population Up to approximately 30 months after first participant enrolled | Arm A: Atezolizumab + Paclitaxel + Carboplatin | 5.6 Months |
| Arm B: Atezolizumab + Nab-Paclitaxel + Carboplatin | 6.5 Months | |||
| Arm C: Nab-Paclitaxel + Carboplatin | 5.6 Months | |||
| NCT02409342 | — | Overall Survival (OS) in the TC2/3 or IC2/3-WT and TC1/2/3 or IC1/2/3-WT Populations From randomization to death from any cause until data cut-off on 4 February 2020 (up to approximately 54.5 months) | Atezolizumab | 19.9 Months |
| Atezolizumab | 18.9 Months | |||
| Chemotherapy (Carboplatin/ Cisplatin) + (Pemetrexed/ Gemcitabine) | 16.1 Months | |||
| Chemotherapy (Carboplatin/ Cisplatin) + (Pemetrexed/ Gemcitabine) | 14.7 Months | |||
| NCT02409342 | — | Overall Survival (OS) in the TC3 or IC3-WT Populations From randomization to death from any cause until data cut-off on 10 September 2018 (up to approximately 38 months) | Atezolizumab | 20.2 Months |
| Chemotherapy (Carboplatin/ Cisplatin) + (Pemetrexed/ Gemcitabine) | 13.1 Months | |||
| NCT02420821 IMmotion151 | Carcinoma, Renal Cell | Overall Survival (OS) in ITT Population Baseline until death from any cause (until data cut-off date 14 February 2020, up to approximately 57 months) | Atezolizumab + Bevacizumab | 36.1 months |
| Sunitinib | 35.3 months | |||
| NCT02420821 IMmotion151 | Carcinoma, Renal Cell | Percentage of Participants Who Died of Any Cause in ITT Population Baseline until death from any cause (until data cut-off date 14 February 2020, up to approximately 57 months) | Atezolizumab + Bevacizumab | 54.8 percentage of participants |
| Sunitinib | 55.3 percentage of participants | |||
| NCT02420821 IMmotion151 | Carcinoma, Renal Cell | Percentage of Participants With Disease Progression as Determined by the Investigator According to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) or Death From Any Cause in Programmed Death-Ligand 1 (PD-L1)-Selected Population Baseline until documented PD or death, whichever occurred first (until data cut-off date 29 September 2017, up to approximately 24 months) | Atezolizumab + Bevacizumab | 58.4 percentage of participants |
| Sunitinib | 69.6 percentage of participants | |||
| NCT02420821 IMmotion151 | Carcinoma, Renal Cell | Progression-Free Survival (PFS) as Determined by the Investigator According to RECIST v1.1 in PD-L1-Selected Population Baseline until documented PD or death, whichever occurred first (until data cut-off date 29 September 2017, up to approximately 24 months) | Atezolizumab + Bevacizumab | 11.2 months |
| Sunitinib | 7.5 months | |||
| NCT02425891 | Triple Negative Breast Neoplasms | OS in Participants With Detectable PD-L1 Baseline until death due to any cause (up to approximately 58 months) | Atezolizumab Plus Nab-Paclitaxel | 25.43 Months |
| Placebo Plus Nab-Paclitaxel | 17.91 Months | |||
| NCT02425891 | Triple Negative Breast Neoplasms | Overall Survival (OS) in All Randomized Participants Baseline until death due to any cause (up to approximately 58 months) | Atezolizumab Plus Nab-Paclitaxel | 21.03 Months |
| Placebo Plus Nab-Paclitaxel | 18.73 Months | |||
| NCT02425891 | Triple Negative Breast Neoplasms | PFS According to RECIST v1.1 in Participants With Detectable Programmed Death-Ligand 1 (PD-L1) Baseline up to approximately 34 months | Atezolizumab Plus Nab-Paclitaxel | 7.46 Months |
| Placebo Plus Nab-Paclitaxel | 4.96 Months | |||
| NCT02425891 | Triple Negative Breast Neoplasms | Progression Free Survival (PFS) According to Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 (v1.1) in All Randomized Participants Baseline up to approximately 34 months | Atezolizumab Plus Nab-Paclitaxel | 7.16 Months |
| Placebo Plus Nab-Paclitaxel | 5.49 Months | |||
| NCT02450331 IMvigor010 | Carcinoma, Transitional Cell | Disease-Free Survival (DFS), as Assessed by Investigator Randomization up to first occurrence of DFS event (up to approximately 50 months) | Atezolizumab | 19.4 Months |
| Observation | 16.6 Months | |||
| NCT02486718 | Carcinoma, Non-Small-Cell Lung | DFS in All Randomized Stage II-IIIA Population Up to 95 months | Atezolizumab | 57.4 months |
| Best Supportive Care (BSC) | 40.8 months | |||
| NCT02486718 | Carcinoma, Non-Small-Cell Lung | DFS in the Programmed Death-ligand 1 (PD-L1) SP263 ≥ 1% Tumor Cell (TC) Subpopulation Within the Stage II-IIIA Population Up to 95 months | Atezolizumab | 68.5 months |
| Best Supportive Care (BSC) | 37.3 months | |||
| NCT02486718 | Carcinoma, Non-Small-Cell Lung | Disease-Free Survival (DFS) in Intent-to-treat (ITT) Population Up to 95 months | Atezolizumab | 65.6 months |
| Best Supportive Care (BSC) | 47.8 months | |||
| NCT02657434 | Carcinoma, Non-Small-Cell Lung | Overall Survival (OS) Randomization up to approximately 39 months | Arm A (Atezolizumab + Carboplatin or Cisplatin + Pemetrexed | 17.5 Months |
| Arm B (Carboplatin or Cisplatin + Pemetrexed) | 13.6 Months | |||
| NCT02657434 | Carcinoma, Non-Small-Cell Lung | Progression Free Survival (PFS) as Assessed by the Investigator Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) Randomization up to approximately 39 months | Arm A (Atezolizumab + Carboplatin or Cisplatin + Pemetrexed | 7.7 Months |
| Arm B (Carboplatin or Cisplatin + Pemetrexed) | 5.2 Months | |||
| NCT02763579 IMpower133 | Small Cell Lung Carcinoma | Duration of Overall Survival (OS) in the Global Population Baseline until death from any cause (up to approximately 23 months) | Atezolizumab + Carboplatin + Etoposide | 12.3 Months (±10.8 95% Confidence Interval) |
| Placebo + Carboplatin + Etoposide | 10.3 Months (±9.3 95% Confidence Interval) | |||
| NCT02763579 IMpower133 | Small Cell Lung Carcinoma | Duration of Progression-Free Survival (PFS) as Assessed by the Investigator Using RECIST v1.1 in the Global Population Baseline until PD or death, whichever occurs first (up to approximately 23 months) | Atezolizumab + Carboplatin + Etoposide | 5.2 Months (±4.4 95% Confidence Interval) |
| Placebo + Carboplatin + Etoposide | 4.3 Months (±4.2 95% Confidence Interval) | |||
| NCT02788279 | Colorectal Neoplasms | Overall Survival (OS) From randomization up to death due to any cause (up to approximately 20 months) | Atezolizumab | 7.10 months |
| Cobimetinib + Atezolizumab | 8.87 months | |||
| Regorafenib | 8.51 months | |||
| NCT02807636 IMvigor130 | Carcinoma, Transitional Cell | Investigator Assessed Progression-Free Survival (PFS) in the Placebo+Gemcitabine+Carboplatin/Cisplatin Arm Versus Atezolizumab +Gemcitabine+Carboplatin/Cisplatin Arm Baseline up to first documented disease progression or death, whichever occurs first (up to approximately 35 months) | Atezolizumab+Gemcitabine+Carboplatin/Cisplatin | 8.18 Months |
| Placebo+Gemcitabine+Carboplatin/Cisplatin | 6.34 Months | |||
| NCT02807636 IMvigor130 | Carcinoma, Transitional Cell | Overall Survival (OS) in Atezolizumab Monotherapy Arm Versus Placebo+Gemcitabine+Carboplatin/Cisplatin Arm Baseline until death due to any cause (up to approximately 73 months) | Atezolizumab Monotherapy | 15.21 Months |
| Placebo+Gemcitabine+Carboplatin/Cisplatin | 13.34 Months | |||
| NCT02807636 IMvigor130 | Carcinoma, Transitional Cell | Overall Survival (OS) in Atezolizumab+Gemcitabine+Carboplatin/Cisplatin Arm Versus Placebo+Gemcitabine+Carboplatin/Cisplatin Arm Baseline until death due to any cause (up to approximately 73 months) | Atezolizumab+Gemcitabine+Carboplatin/Cisplatin | 16.13 Months |
| Placebo+Gemcitabine+Carboplatin/Cisplatin | 13.44 Months | |||
| NCT02839707 | Ovarian Neoplasms | Incidence of Dose Limiting Toxicities (DLT) of Experimental Regimens Up to 28 days | Arm I (PLD, Atezolizumab) | 0 Participants |
| Arm II (PLD, Bevacizumab, Atezolizumab) | 0 Participants | |||
| Arm III (PLD, Bevacizumab) | 0 Participants | |||
| NCT02839707 | Ovarian Neoplasms | Overall Survival (OS) (Phase III) From study enrollment to the date of death regardless of the cause, assessed up to 5 years | Arm I (PLD, Atezolizumab) | 14.5 months |
| Arm II (PLD, Bevacizumab, Atezolizumab) | 14.9 months | |||
| Arm III (PLD, Bevacizumab) | 12.3 months | |||
| NCT02839707 | Ovarian Neoplasms | PFS (Phase III) From study enrollment to the investigator determined date of progression or death due to any cause, whichever occurs first, assessed up to 5 years. | Arm I (PLD, Atezolizumab) | 4.0 months |
| Arm II (PLD, Bevacizumab, Atezolizumab) | 7.4 months | |||
| Arm III (PLD, Bevacizumab) | 5.6 months | |||
| NCT02839707 | Ovarian Neoplasms | Progression Free Survival (PFS) (Phase II) From study enrollment to the investigator determined date of progression or death due to any cause, whichever occurs first, assessed up to 5 years | Arm I (PLD, Atezolizumab) | 4.2 months |
| Arm II (PLD, Bevacizumab, Atezolizumab) | 7.6 months | |||
| Arm III (PLD, Bevacizumab) | 5.5 months | |||
| NCT02908672 | Melanoma | Progression-Free Survival (PFS), as Determined by Investigator Using Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 Baseline up to PD or death due to any cause, whichever occurred first (up to approximately 33 months) | Arm A: Pbo + Cobi + Vem | 10.6 months |
| Arm B: Atezo + Cobi + Vem | 15.1 months | |||
| NCT02912559 | Colonic Neoplasms | Disease Free Survival (DFS) 3 years | Arm I (Combination Chemotherapy, Atezolizumab) | 86.3 percentage of participants |
| Arm II (Combination Chemotherapy) | 76.2 percentage of participants | |||
| NCT02928406 | Urologic Neoplasms | Percentage of Participants With Adverse Events (AEs) Baseline up to end of study (up to approximately 6 years) | Atezolizumab | 900 Participants |
| NCT03016312 IMbassador250 | Prostatic Neoplasms, Castration-Resistant | Overall Survival (OS) Baseline until death from any cause (up to approximately 42 months) | Atezolizumab + Enzalutamide | 15.2 Months |
| Enzalutamide | 16.6 Months | |||
| NCT03024996 IMmotion010 | Carcinoma, Renal Cell | Investigator-assessed Disease-Free Survival (DFS) From baseline up to first occurence of event by investigator assessment (up to approximately 64 months) | Atezolizumab | 57.2 Months |
| Placebo | 49.5 Months | |||
| NCT03038100 IMagyn050 | Ovarian Neoplasms | Overall Survival - ITT Population From randomization up to death from any cause (up to approximately 59 months) | Atezolizumab With Paclitaxel, Carboplatin and Bevacizumab | 50.53 Months |
| Placebo With Paclitaxel, Carboplatin and Bevacizumab | 46.59 Months | |||
| NCT03038100 IMagyn050 | Ovarian Neoplasms | Overall Survival - PD-L1-Positive Subpopulation From randomization up to death from any cause (up to approximately 59 months) | Atezolizumab With Paclitaxel, Carboplatin and Bevacizumab | NA Months |
| Placebo With Paclitaxel, Carboplatin and Bevacizumab | 49.15 Months | |||
| NCT03038100 IMagyn050 | Ovarian Neoplasms | PFS Assessed by Investigator as Per RECIST v1.1 - Programmed Death-Ligand 1 (PD-L1)-Positive Subpopulation From randomization until disease progression or death from any cause (up to approximately 55 months) | Atezolizumab With Paclitaxel, Carboplatin and Bevacizumab | 20.83 Months |
| Placebo With Paclitaxel, Carboplatin and Bevacizumab | 18.50 Months | |||
| NCT03038100 IMagyn050 | Ovarian Neoplasms | Progression-Free Survival (PFS) Assessed by Investigator as Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) - Intent-to-Treat (ITT) Population From randomization until disease progression or death from any cause (up to approximately 55 months) | Atezolizumab With Paclitaxel, Carboplatin and Bevacizumab | 19.48 Months |
| Placebo With Paclitaxel, Carboplatin and Bevacizumab | 18.37 Months | |||
| NCT03125902 IMpassion131 | Triple Negative Breast Neoplasms | Progression-Free Survival (PFS) Assessed Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) in the Intent-to-Treat (ITT) Population From Day 1 to disease progression (PD) or death from any cause, assessed up to primary completion date (approximately 26 months) | Atezolizumab and Paclitaxel | 5.68 Months |
| Placebo and Paclitaxel | 5.55 Months | |||
| NCT03125902 IMpassion131 | Triple Negative Breast Neoplasms | Progression-Free Survival (PFS) Assessed Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) in the Subpopulation With Programmed Death-Ligand 1 (PD-L1)-Positive Tumour Status From Day 1 to disease progression (PD) or death from any cause, assessed up to primary completion date (approximately 26 months) | Atezolizumab and Paclitaxel | 5.95 Months |
| Placebo and Paclitaxel | 5.72 Months | |||
| NCT03191786 IPSOS | Carcinoma, Non-Small-Cell Lung | Overall Survival (OS) From randomization up to death from any cause (up to approximately 55 months) | Atezolizumab | 10.3 Months |
| Single Agent Chemotherapy (Vinorelbine or Gemcitabine) | 9.2 Months | |||
| NCT03197935 IMpassion031 | Triple Negative Breast Neoplasms | Number of Participants With Pathologic Complete Response (pCR) Using American Joint Committee on Cancer (AJCC) Staging System in ITT Population After neoadjuvant study treatment and surgery, up to primary analysis data cut off on 03 ApriI 2020 | Atezolizumab and Chemotherapy | 95 Number of Participants |
| Placebo and Chemotherapy | 69 Number of Participants | |||
| NCT03197935 IMpassion031 | Triple Negative Breast Neoplasms | Number of Participants With pCR in Subpopulation With PD-L1-Positive Tumor Status (Tumor-infiltrating Immune Cell [IC] 1/2/3) Using AJCC Staging System After neoadjuvant study treatment and surgery, up to primary analysis data cut off on 03 ApriI 2020 | Atezolizumab and Chemotherapy | 53 Number of Participants |
| Placebo and Chemotherapy | 37 Number of Participants | |||
| NCT03199885 | Breast Neoplasms | Progression-Free Survival (PFS) At the definitive analysis 2.5 years | Arm I (Pertuzumab, Trastuzumab, Taxane Therapy, Placebo) | 40.5 percentage of participants |
| Arm II (Pertuzumab, Trastuzumab, Taxane Therapy, Atezolizumab) | 52.3 percentage of participants | |||
| NCT03273153 | — | Progression Free Survival (PFS) as Determined by the Independent Review Committee (IRC) Every 8 weeks (wks) from Day (D) 1 of Cycle (C) 1 through approximately 16 months | Cobimetinib and Atezolizumab | 5.5 Months |
| Pembrolizumab | 5.7 Months | |||
| NCT03371017 IMpassion132 | Triple Negative Breast Neoplasms | OS in Modified Intent-to-treat (mITT) Population Time from randomization to death (Up to 68 months) | Atezolizumab + Chemotherapy | 10.35 months |
| Placebo + Chemotherapy | 9.79 months | |||
| NCT03371017 IMpassion132 | Triple Negative Breast Neoplasms | Overall Survival (OS) in PD-L1-positive Population Time from randomization to death (Up to 68 months) | Atezolizumab + Chemotherapy | 12.09 months |
| Placebo + Chemotherapy | 11.24 months | |||
| NCT03434379 IMbrave150 | Carcinoma, Hepatocellular | Overall Survival (OS) in the China Population From randomization to death from any cause up to the clinical cut off date (CCOD) of 29Aug2019 (up to approximately 18 months) and 31Aug2020 (up to approximately 30 months) | Atezolizumab + Bevacizumab - China | 24.05 months |
| Atezolizumab + Bevacizumab - China | NA months | |||
| Sorafenib - China | 11.37 months | |||
| Sorafenib - China | 11.37 months | |||
| NCT03434379 IMbrave150 | Carcinoma, Hepatocellular | Overall Survival (OS) in the Global Population From randomization to death from any cause up to the clinical cut off date (CCOD) of 29Aug2019 (up to approximately 18 months) and 31Aug2020 (up to approximately 30 months) | Atezolizumab + Bevacizumab - Global | NA months |
| Atezolizumab + Bevacizumab - Global | 19.22 months | |||
| Sorafenib - Global | 13.40 months | |||
| Sorafenib - Global | 13.24 months | |||
| NCT03434379 IMbrave150 | Carcinoma, Hepatocellular | PFS-IRF Per RECIST v1.1 in the China Population Randomization to the first occurrence of disease progression or death from any cause up to CCOD of 29Aug2019 (up to approximately 18 months) | Atezolizumab + Bevacizumab - China | 5.72 months |
| Sorafenib - China | 3.19 months | |||
| NCT03434379 IMbrave150 | Carcinoma, Hepatocellular | Progression Free Survival by Independent Review Facility-Assessment (PFS-IRF) Per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 in the Global Population Randomization to the first occurrence of disease progression or death from any cause up to CCOD of 29Aug2019 (up to approximately 18 months) | Atezolizumab + Bevacizumab - Global | 6.83 months |
| Sorafenib - Global | 4.27 months | |||
| NCT03452137 IMvoke010 | — | Investigator-Assessed Event-Free Survival (INV-assessed EFS) Randomization to the first documented disease recurrence, disease progression or death from any cause, whichever occurs first (up to 5 years) | Atezolizumab | 59.47 months |
| Placebo | 52.73 months | |||
| NCT03498716 IMpassion030 | Triple Negative Breast Neoplasms | Invasive Disease-Free Survival (iDFS) From randomization until the occurrence of an iDFS event or death from any cause, whichever occurred earlier (up to 5 years) | Atezolizumab and Chemotherapy | NA months |
| Chemotherapy | NA months | |||
| NCT03726879 IMpassion050 | Breast Neoplasms | pCR in the ITT Population From randomization to approximately 6 months | Atezolizumab +ddAC-PacHP | 62.4 Percentage of Participants |
| Placebo + ddAC-PacHP | 62.7 Percentage of Participants | |||
| NCT03726879 IMpassion050 | Breast Neoplasms | Percentage of Participants With Pathological Complete Response (pCR) in the PD-L1-Positive Population (IC 1/2/3) From randomization to approximately 6 months | Atezolizumab +ddAC-PacHP | 64.2 Percentage of Participants |
| Placebo + ddAC-PacHP | 72.5 Percentage of Participants | |||
| NCT03735121 | Carcinoma, Non-Small-Cell Lung | Part 1: Serum Trough Concentration (Ctrough) of Atezolizumab at Cycle 1 Pre-dose on Day 1 of Cycle 2 (Cycle length=21 days for cohorts 1 and 3 and 14 days for cohort 2) | Part 1 Cohort 1: Atezolizumab SC Co-mix 1800 mg | 121 micrograms per milliliter (μg/mL) (±42.8 Geometric Coefficient of Variation) |
| Part 1 Cohort 2: Atezolizumab SC Co-mix 1200 mg | 77.5 micrograms per milliliter (μg/mL) (±51.4 Geometric Coefficient of Variation) | |||
| Part 1 Cohort 3: Atezolizumab SC Co-mix 1800 mg | 78.3 micrograms per milliliter (μg/mL) (±88.6 Geometric Coefficient of Variation) | |||
| NCT03735121 | Carcinoma, Non-Small-Cell Lung | Part 2: Area Under the Concentration-Time Curve From Time Zero to 21 Days (AUC 0-21 d) at Cycle 1 From start of dosing up to Day 21 in Cycle 1 (Cycle length = 21 days) | Part 2: Atezolizumab IV 1200 mg | 3327.9 micrograms day per mL (μg*day/mL) (±19.4 Geometric Coefficient of Variation) |
| Part 2: Atezolizumab SC 1875 mg | 2907.1 micrograms day per mL (μg*day/mL) (±35.9 Geometric Coefficient of Variation) | |||
| NCT03735121 | Carcinoma, Non-Small-Cell Lung | Part 2: Observed Serum Ctrough of Atezolizumab at Cycle 1 Predose on Day 1 of Cycle 2 (Cycle length =21 days) | Part 2: Atezolizumab IV 1200 mg | 85.4 μg/mL (±34.1 Geometric Coefficient of Variation) |
| Part 2: Atezolizumab SC 1875 mg | 89.4 μg/mL (±127.1 Geometric Coefficient of Variation) | |||
| NCT03755791 COSMIC-312 | Carcinoma, Hepatocellular | Overall Survival (OS) for the Experimental Arm Versus the Control Arm in the ITT Population From the date of first participant randomization up to 36 months | Control Arm: Sorafenib | 15.51 months |
| Experimental Arm: Cabozantinib + Atezolizumab | 16.46 months | |||
| NCT03755791 COSMIC-312 | Carcinoma, Hepatocellular | Progression Free Survival (PFS) for the Experimental Arm Versus the Control Arm in the PFS Intent to Treat (PITT) Population From the date of first participant randomization up to 28 months | Control Arm: Sorafenib | 4.21 months |
| Experimental Arm: Cabozantinib + Atezolizumab | 6.80 months | |||
| NCT03811002 | Lung Neoplasms | Overall Survival Randomization to date of death due or last follow-up. Median follow-up at the time of analysis was 23.8 months. | Arm I (Chemotherapy, Radiation Therapy) | 36.1 months |
| Arm II (Chemotherapy, Radiation Therapy, Atezolizumab) | 31.1 months | |||
| NCT04102098 IMbrave050 | Carcinoma, Hepatocellular | Recurrence-Free Survival (RFS), as Determined by IRF Baseline up to approximately 33 months | Arm A (Atezolizumab Plus Bevacizumab) | NA Months |
| Arm B (Active Surveillance) | NA Months | |||
| NCT04148911 EL1SSAR | Triple Negative Breast Neoplasms | Percentage of Participants With Treatment-emergent Grade ≥2 Immune-mediated AEs (imAEs) Up to 60 months | Atezolizumab + Nab-paclitaxel | 12.09 percentage of participants |
| NCT04148911 EL1SSAR | Triple Negative Breast Neoplasms | Percentage of Participants With Treatment-emergent Grade ≥3 Adverse Events (AEs) Up to 60 months | Atezolizumab + Nab-paclitaxel | 46.70 percentage of participants |
| NCT04177108 | Neoplasms | Overall Survival (OS) From randomization up to study completion or death (Up to 39 months) | Cohort 1 Arm A: Ipatasertib + Atezolizumab + Paclitaxel | 15.7 months |
| Cohort 1 Arm B: Ipatasertib + Atezolizumab Matching Placebo + Paclitaxel | 15.3 months | |||
| Cohort 1 Arm C: Ipatasertib Matching Placebo + Atezolizumab Matching Placebo + Paclitaxel | 16.6 months | |||
| Cohort 2 Arm A: Ipatasertib + Atezolizumab + Paclitaxel | NA months | |||
| Cohort 2 Arm B: Ipatasertib Matching Placebo+ Atezolizumab + Paclitaxel | 17.2 months | |||
| NCT04177108 | Neoplasms | Progression-Free Survival (PFS) According to Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 From Randomization to disease progression, study completion, or death (up to 39 months) | Cohort 1 Arm A: Ipatasertib + Atezolizumab + Paclitaxel | 7.1 months |
| Cohort 1 Arm B: Ipatasertib + Atezolizumab Matching Placebo + Paclitaxel | 5.6 months | |||
| Cohort 1 Arm C: Ipatasertib Matching Placebo + Atezolizumab Matching Placebo + Paclitaxel | 3.7 months | |||
| Cohort 2 Arm A: Ipatasertib + Atezolizumab + Paclitaxel | 5.6 months | |||
| Cohort 2 Arm B: Ipatasertib Matching Placebo+ Atezolizumab + Paclitaxel | 5.7 months | |||
| NCT04256421 SKYSCRAPER-02 | Small Cell Lung Carcinoma | Investigator-assessed Progression-free Survival (PFS) in the Primary Analysis Set (PAS) From randomization to the first occurrence of PD or death from any cause, whichever occurred first (up to approximately 24 months) | Arm A: Placebo + Atezolizumab | 5.55 months |
| Arm B: Tiragolumab + Atezolizumab | 5.36 months | |||
| NCT04256421 SKYSCRAPER-02 | Small Cell Lung Carcinoma | Overall Survival (OS) in the PAS From randomization to death from any cause (up to approximately 24 months) | Arm A: Placebo + Atezolizumab | 13.14 months |
| Arm B: Tiragolumab + Atezolizumab | 13.11 months | |||
| NCT04338269 CONTACT-03 | Carcinoma, Renal Cell | Overall Survival (OS) From randomization to death due to any cause (up to 2 years 5 months). | Atezolizumab + Cabozantinib | 25.72 months |
| Cabozantinib (Control) | NA months | |||
| NCT04338269 CONTACT-03 | Carcinoma, Renal Cell | Progression Free Survival (PFS) as Assessed by an Independent Review Facility (IRF) (IRF-PFS) According to RECIST v1.1 From randomization to the first occurrence of PD according to RECIST v1.1, or death from any cause, whichever occurred first (up to 2 years 5 months) | Atezolizumab + Cabozantinib | 10.55 months |
| Cabozantinib (Control) | 10.81 months | |||
| NCT04446117 CONTACT-02 | Prostatic Neoplasms | Duration of Overall Survival (OS) Up to a maximum of approximately 45 months (Median duration of follow-up was 24.05 months) | Control Arm: Second NHT | 14.98 months |
| Experimental Arm: Cabozantinib and Atezolizumab | 14.78 months | |||
| NCT04446117 CONTACT-02 | Prostatic Neoplasms | Duration of Progression Free Survival (PFS) Per Response Evaluable Criteria in Solid Tumors Version 1.1 (RECIST 1.1) by Blinded Independent Radiology Committee (BIRC) Up to a maximum of approximately 30 months (Median duration of follow-up was 14.31 months) | Control Arm: Second NHT | 4.17 months |
| Experimental Arm: Cabozantinib and Atezolizumab | 6.34 months | |||
| NCT04471428 CONTACT-01 | Carcinoma, Non-Small-Cell Lung | Overall Survival (OS) Up to approximately 24 months | Atezolizumab + Cabozantinib | 10.7 months |
| Docetaxel Monotherapy | 10.5 months | |||
| NCT04487067 AMETHISTA | Carcinoma, Hepatocellular | Number of Participants With Grade 3-5 National Cancer Institute Common Terminology Criteria for Adverse Events, Version 5.0 (NCI CTCAE V5) Bleeding/Haemorrhage Up to approximately 47.6 months | Atezolizumab + Bevacizumab | 17 Participants |
| Atezolizumab + Bevacizumab | 2 Participants | |||
| Atezolizumab + Bevacizumab | 3 Participants | |||
| NCT04540211 SKYSCRAPER-08 | Esophageal Neoplasms | Independent Review Facility (IRF)-Assessed Progression-Free Survival (PFS) From randomization to the first occurrence of disease progression or death from any cause, whichever occurs first (up to approximately 19 months) | Atezolizumab + Tiragolumab + PC | 6.18 months |
| Placebo + PC | 5.39 months | |||
| NCT04540211 SKYSCRAPER-08 | Esophageal Neoplasms | Overall Survival (OS) From randomization to death from any cause (up to approximately 27 months) | Atezolizumab + Tiragolumab + PC | 15.74 months |
| Placebo + PC | 11.10 months | |||
| NCT04637594 IMAGINE | Carcinoma, Transitional Cell | Overall Survival (OS) Rate at 12 Months 12 months | Arm A (Immune Checkpoint Inhibitor) | 0 percentage of participants |
| Arm B (Immune Checkpoint Inhibitor) | 0 percentage of participants | |||
| NCT04665856 SKYSCRAPER-02C | Small Cell Lung Carcinoma | Investigator-Assessed Progression-Free Survival (PFS) in the Primary Analysis Set (PAS) Up to 32.3 months | Placebo + Atezolizumab + Carboplatin + Etoposide | 5.39 months |
| Tiragolumab + Atezolizumab + Carboplatin + Etoposide | 5.59 months | |||
| NCT04665856 SKYSCRAPER-02C | Small Cell Lung Carcinoma | Overall Survival (OS) in the PAS Up to 32.3 months | Placebo + Atezolizumab + Carboplatin + Etoposide | 13.54 months |
| Tiragolumab + Atezolizumab + Carboplatin + Etoposide | 18.69 months | |||
| NCT04732286 | Carcinoma, Hepatocellular | Number of Participants Who Discontinued Atezolizumab and/or Bevacizumab Due to Adverse Events (AE) of Grade ≥ 3 From Cycle 1 Day 1 up to 30 days after the final dose of the study drug or until initiation of another anti-cancer therapy, whichever occurred first (up to approximately 32 months) | Atezolizumab + Bevacizumab | 19 Participants |
| NCT04740918 KATE3 | Breast Neoplasms | Overall Survival (OS) Up to 28 months | Trastuzumab Emtansine 3.6 mg + Atezolizumab 1200 mg | NA months |
| Trastuzumab Emtansine 3.6 mg + Placebo | NA months | |||
| NCT04740918 KATE3 | Breast Neoplasms | Progression-Free Survival (PFS) as Determined by Investigator Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) Up to 28 months | Trastuzumab Emtansine 3.6 mg + Atezolizumab 1200 mg | 8.61 months |
| Trastuzumab Emtansine 3.6 mg + Placebo | 7.52 months | |||
| NCT05091567 IMforte | Small Cell Lung Carcinoma | Randomized Phase: Independent Review Facility (IRF) - Assessed Progression Free Survival (PFS) Up to 26 months | Atezolizumab | 2.14 months (±1.64 95% Confidence Interval) |
| Atezolizumab+ Lurbinectedin | 5.36 months (±4.24 95% Confidence Interval) | |||
| NCT05091567 IMforte | Small Cell Lung Carcinoma | Randomized Phase: Overall Survival (OS) Up to 26 months | Atezolizumab | 10.64 months (±9.49 95% Confidence Interval) |
| Atezolizumab+ Lurbinectedin | 13.24 months (±11.89 95% Confidence Interval) | |||
| NCT05224141 | Small Cell Lung Carcinoma | Overall Survival (OS) Up to approximately 25 months | Atezolizumab | 12.9 Months |
| Pembrolizumab/Vibostolimab | 11.5 Months | |||
| NCT05694013 ORIGAMA | Neoplasms | Mean Difference in Change of Week 12 Value From Baseline of Participant-reported Total Symptom Interference Score From the MD Anderson Symptom Inventory (MDASI) Core Items Baseline, Week 12 | Atezolizumab Regimen | 3.00 Units on a scale |
| Atezolizumab Regimen | 3.33 Units on a scale | |||
| Atezolizumab Regimen + DPM | 3.08 Units on a scale | |||
| Atezolizumab Regimen + DPM | 2.33 Units on a scale |