A Phase 3 Randomized, Double-Blind, Placebo-controlled Study in Older Subjects to Assess Safety and the Reversal of Apixaban Anticoagulation With Intravenously Administered Andexanet Alfa
Latest Information Update: 07 Nov 2021
At a glance
- Drugs Andexanet alfa (Primary) ; Apixaban
- Indications Haemorrhage
- Focus Registrational; Therapeutic Use
- Acronyms ANNEXA-A
- Sponsors Portola Pharmaceuticals
- 26 Apr 2019 According to a Portola Pharmaceuticals media release, based on results of ANNEXA-R, ANNEXA-A and ANNEXA-4 (n=352), studies, the European Commission (EC) has granted conditional Marketing Authorization of Ondexxya (andexanet alfa) for the treatment of the adult patients with the Factor Xa inhibitor apixaban or rivaroxaban when reversal of anticoagulation is needed due to life-threatening or uncontrolled bleeding.
- 01 Mar 2019 According to a Portola Pharmaceuticals media release, the CHMP has recommended that the European Commission (EC) grant Ondexxya conditional approval for the reversal of the anticoagulant effects of the Factor Xa inhibitors apixaban or rivaroxaban in patients experiencing uncontrolled or life-threatening bleeding. The EC is expected to issue a decision in early May 2019.
- 01 Mar 2019 According to a Portola Pharmaceuticals media release, based on results of this study, the Committee for Medicinal Products for Human Use (CHMP) of the EMA has adopted a positive opinion on the marketing authorization application (MAA) for Ondexxya (andexanet alfa).
Most Recent Events
Trial Overview
Outcome
Purpose
This pivotal trial investigated the efficacy and tolerability of andexanet alfa [PRT 4445] for the reversal of apixaban-induced anticoagulation in healthy older volunteers.
The trial was conducted in two parts. In the first part, 33 participants received apixaban 5mg twice daily for 3.5 days and were then randomised 3:1 to receive andexanet alfa as a 400mg IV bolus (n = 24) or placebo (n = 9). In the second part, 31 participants received apixaban 5mg twice daily for 4 days and were then randomised 3:1 to receive andexanet alfa as a 400mg IV bolus followed by continuous infusion of 4 mg/min for 120 minutes (n = 23) or to receive placebo (n = 8).
Comments
According to a Portola Pharmaceuticals media release, based on results of ANNEXA-R, ANNEXA-A and ANNEXA-4 (n=352), studies, the European Commission (EC) has granted conditional Marketing Authorization of Ondexxya (andexanet alfa) for the treatment of the adult patients with the Factor Xa inhibitor apixaban or rivaroxaban when reversal of anticoagulation is needed due to life-threatening or uncontrolled bleeding.
Based on the results of ANNEXA-R, ANNEXA-A and interim data from ANNEXA-4 (n=185), the U.S. Food and Drug Administration (FDA) has approved Andexxa, the first and only antidote for patients treated with rivaroxaban and apixaban, in reversing the anticoagulant activity of the Factor Xa inhibitors.
Primary Endpoints
Reversal of Apixaban anticoagulation effect as measured by anti-factor Xa activity [1]
Other Endpoints
Efficacy: Percent Change From Baseline in Anti-fXa Activity at the Nadir (Part II)
description: The percent change from baseline in anti-fXa activity at the nadir, following the bolus, when nadir was defined as the smaller value for anti-fXa activity at the +2 minute or +5 minute time point after the completion of the andexanet bolus (Part II). Baseline was the last assessment obtained prior to the first dose of andexanet or placebo time_frame: Baseline to +2 minutes or +5 minutes following the end of andexanet/placebo bolus (Part II)
Efficacy: Number of Participants With ≥80% Reduction in the Anti-fXa Activity From Baseline to Nadir
description: Occurrence of ≥80% reduction in anti-fXa activity from its baseline to nadir, when nadir was defined as the smaller value for anti-fXa activity at the +2 minute or +5 minute time point after the completion of the andexanet bolus (Part I) or between the 110-minute time point (10 minutes prior to the end of the continuous infusion) and the 5-minute time point after the end of the continuous infusion (inclusive) [Part II]. Baseline was the last assessment obtained prior to the first dose of andexanet or placebo time_frame: Baseline to +2 minutes or +5 minutes following the end of andexanet/placebo bolus (Part I), or 10 minutes prior to end of andexanet/placebo continuous infusion or 5 minutes after the end of andexanet/placebo continuous infusion (Part II)
Efficacy -Change From Baseline in Free Apixaban Concentration at the Nadir
description: Change from baseline in free apixaban concentration (ng/mL) at the nadir, when nadir was defined as the smaller value for free apixaban at the +2 minute or +5 minute time point after the completion of the andexanet bolus (Part I) or between the 110-minute time point (10 minutes prior to the end of the continuous infusion) and the 5-minute time point after the end of the continuous infusion (inclusive) [Part II]. Free plasma concentrations of apixaban was determined using a validated method that involved analysis of citrated human plasma with high-throughput equilibrium dialysis followed by liquid chromatography mass spectrometry. time_frame: Baseline to +2 minutes or +5 minutes following the end of andexanet/placebo bolus (Part I), or 10 minutes prior to end of andexanet/placebo continuous infusion or 5 minutes after the end of andexanet/placebo continuous infusion (Part II)
Efficacy: Change in Thrombin Generation (ETP) From Baseline to Its Peak [Parts I and II]
description: Change in ETP from baseline to its peak, where peak was defined as the largest value for ETP between the +2 minute time point and the +10 minute time point after the end of the andexanet bolus (inclusive) {Part I] or between the 110-minute time point (10 minutes prior to the end of the continuous infusion) and the 5-minute time point after the end of the continuous infusion (inclusive) [Part II]. Baseline was the last assessment obtained prior to the first dose of andexanet or placebo. ETP was measured using a tissue factor-initiated thrombin generation assay. time_frame: Baseline to +2 minutes or +10 minutes following the end of andexanet/placebo bolus (Part I), or 10 minutes prior to end of andexanet/placebo continuous infusion or 5 minutes after the end of andexanet/placebo continuous infusion (Part II)
Efficacy: Number of Participants With Thrombin Generation (ETP) Above the Lower Limit of the Derived Normal Range at Its Peak (mITT Population)
description: Number of participants with ETP above the lower limit of the normal range at its peak, between the +2 minute time point and the +10 minute time point after the end of the andexanet bolus (inclusive) [Part I] or between the 110-minute time point (10 minutes prior to the end of the continuous infusion) and the 5-minute time point after the end of the continuous infusion (inclusive) [Part II]. ETP was measured using a tissue factor-initiated thrombin generation assay time_frame: Baseline to +2 minutes or +10 minutes following the end of andexanet/placebo bolus (Part I), or 10 minutes prior to end of andexanet/placebo continuous infusion or 5 minutes after the end of andexanet/placebo continuous infusion (Part II) [2]
Diseases Treated
| Indication | Qualifiers | Patient Segments |
|---|---|---|
| Haemorrhage | prevention | - |
Biomarker
| NCT Number | Biomarker Name | Biomarker Function |
|---|---|---|
| NCT02207725 | Prothrombin (PT) | Outcome Measure |
Subjects
- Subject Type volunteers
-
Number
Planned: 64
Actual: 68
- Sex male & female
- Age Group 50-75 years; adult; elderly
Patient Inclusion Criteria
Reasonably healthy men and women aged 50 to 75
Patient Exclusion Criteria
History of abnormal bleeding, active bleeding or risk factors for bleeding - History of thrombosis or risk factors for thrombosis - History of adult asthma or use of inhaled medications
Trial Details
Identifiers
| Identifier | Owner |
|---|---|
| NCT02207725 | ClinicalTrials.gov: US National Institutes of Health |
| 14-503 | - |
Organisations
- Sponsors Portola Pharmaceuticals
- Affiliations Bristol-Myers Squibb; Pfizer; Portola Pharmaceuticals
Trial Dates
-
Initiation Dates
Planned : 01 Jun 2014
Actual : 19 Mar 2014
-
Primary Completion Dates
Planned : 01 Oct 2014
Actual : 01 Apr 2015
-
End Dates
Planned : 01 Nov 2014
Actual : 01 Sep 2015
Other Details
- Design double-blind; multicentre; parallel; prospective; randomised
- Phase of Trial Phase III
- Location USA
- Focus Registrational; Therapeutic Use
Interventions
| Drugs | Route | Formulation |
|---|---|---|
| Andexanet alfaPrimary Drug | Intravenous | Infusion |
| Apixaban |
-
|
-
|
The trial was conducted in two parts. In the first part, 33 participants received apixaban 5mg twice daily for 3.5 days and were then randomised 3:1 to receive andexanet alfa as a 400mg IV bolus (n = 24) or placebo (n = 9). In the second part, 31 participants received apixaban 5mg twice daily for 4 days and were then randomised 3:1 to receive andexanet alfa as a 400mg IV bolus followed by continuous infusion of 4 mg/min for 120 minutes (n = 23) or to receive placebo (n = 8).
Placebo
Andexanet alfa (part 1)
Andexanet alfa (Dosage: 400mg; Route: IV; Frequency: single dose; Duration: single dose; Company: Portola Pharmaceuticals; In the first part of the study, approximately 32 healthy volunteers will be given apixaban 5 mg twice daily and then randomised in a 3:1 ratio to andexanet alfa administered as a 400 mg IV bolus or to placebo.)
Andexanet alfa (part 2)
Andexanet alfa (Dosage: 400mg; Route: IV; Frequency: single dose; Duration: single dose; Company: Portola Pharmaceuticals; In the second part of the study, approximately 32 healthy volunteers will be randomised in a 3:1 ratio to andexanet alfa administered as a 400 mg IV bolus followed by a continuous infusion of 480 mg at 4 mg/min for 120 minutes or to placebo.)
Andexanet alfa (Dosage: 480mg at 4 mg/min for 120 minutes; Route: IV infusion; Frequency: cont; Duration: single dose; Company: Portola Pharmaceuticals)
Results
Therapeutic efficacy
In older healthy volunteers, compared to placebo, andexanet alfa was associated with a statistically significant reversal of anticoagulant activity of Eliquis (apixaban) by approximately 94% (primary endpoint; p< 0.0001). A significant reduction in the level of free, unbound Eliquis in the plasma was observed. [1] [3]
Adverse events
Pharmacodynamics
Publications
-
Portola Pharmaceuticals. Portola Pharmaceuticals Announces Phase 3 ANNEXA(TM)-A Study of Andexanet Alfa and Eliquis (Apixaban) Met Primary and Secondary Endpoints With High Statistical Significance. Media-Rel 2014;.
Media Release -
Portola Pharmaceuticals, Bristol-Myers Squibb, Pfizer. Portola, Bristol-Myers Squibb and Pfizer Announce Statistically Significant Results From the First Part of the Phase 3 ANNEXA(Tm)-A Studies of Investigational Andexanet Alfa With Eliquis (apixaban). Media-Rel 2014;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Announces New Topline Data From Phase 3 ANNEXA-A(Tm) Trial Part 2: Breakthrough Designated Andexanet Alfa Successfully Meets Primary Endpoint for Prolonged Reversal of Factor Xa Inhibitor Eliquis (apixaban). Media-Rel 2015;.
Media Release -
Crowther M, Gold AM, Lu G, Leeds JM, Wiens BL, Mathur V, et al. Andexanet Alfa, a Universal Antidote for Reversal of Anticoagulation of Factor Xa Inhibitors in Healthy Human Volunteers. ISC-2016 2016; abstr. A212.
Available from: URL: http://stroke.ahajournals.org/content/47/Suppl_1/A212.abstract?sid=f62e60b5-7da6-4a2a-b286-4d2e500f47d547/Suppl_1/A212#cited-by -
Portola Pharmaceuticals. The New England Journal of Medicine Publishes Results of Portola Pharmaceuticals Phase 3 ANNEXA Studies of Andexanet Alfa. Media-Rel 2015;.
Media Release -
Lu G, Lin J, Bronson M, Crowther M, Conley PB, Curnutte JT. Reversal of apixaban and rivaroxaban anticoagulation by andexanet alfa in ANNEXA-A&R as assessed by non-tissue factor (TF)-initiated thrombin generation independent of TF pathway inhibitor (TFPI). ESC-Card-2018 2018; abstr. 5069.
Available from: URL: http://link.adisinsight.com/w8PJo -
Siegal DM, Curnutte JT, Connolly SJ, Lu G, Conley PB, Wiens BL, et al. Andexanet Alfa for the Reversal of Factor Xa Inhibitor Activity. N-Engl-J-Med 2015;.
PubMed | CrossRef Fulltext -
Rogers KC, Finks SW. A New Option for Reversing the Anticoagulant Effect of Factor Xa Inhibitors: Andexanet alfa (Andexxa(R)). Am-J-Med 2018;.
PubMed | CrossRef Fulltext -
Momin JH, Hughes GJ. Andexanet alfa (Andexxa) for the reversal of direct oral anticoagulants. PT 2019;44(9):530-549.
PubMed | CrossRef Fulltext -
Portola Pharmaceuticals, Bristol-Meyers Squibb, Pfizer. Portola, Bristol-Myers Squibb and Pfizer Announce Full Results of Second Part of Phase 3 ANNEXA-A(Tm) Study Demonstrating That Investigational Andexanet Alfa Sustained Reversal of Anticoagulant Effect of Factor Xa Inhibitor Eliquis (apixaban). Media-Rel 2015;.
Media Release
Trial Centres
Centres
| Centre Name | Location | Trial Centre Country |
|---|---|---|
| Celerion | Tempe, Arizona | USA |
| Portola Pharmaceuticals | South San Francisco, California | USA |
Trial History
| Event Date | Event Type | Comment |
|---|---|---|
| 01 Sep 2019 | Results | Results (from ANNEXA-A, ANNEXA-R and ANNEXA-4) published in the P and T Updated 22 Nov 2019 |
| 26 Apr 2019 | Other trial event | According to a Portola Pharmaceuticals media release, based on results of ANNEXA-R, ANNEXA-A and ANNEXA-4 (n=352), studies, the European Commission (EC) has granted conditional Marketing Authorization of Ondexxya (andexanet alfa) for the treatment of the adult patients with the Factor Xa inhibitor apixaban or rivaroxaban when reversal of anticoagulation is needed due to life-threatening or uncontrolled bleeding. Updated 03 May 2019 |
| 01 Mar 2019 | Other trial event | According to a Portola Pharmaceuticals media release, the CHMP has recommended that the European Commission (EC) grant Ondexxya conditional approval for the reversal of the anticoagulant effects of the Factor Xa inhibitors apixaban or rivaroxaban in patients experiencing uncontrolled or life-threatening bleeding. The EC is expected to issue a decision in early May 2019. Updated 08 Mar 2019 |
| 01 Mar 2019 | Other trial event | According to a Portola Pharmaceuticals media release, based on results of this study, the Committee for Medicinal Products for Human Use (CHMP) of the EMA has adopted a positive opinion on the marketing authorization application (MAA) for Ondexxya (andexanet alfa). Updated 08 Mar 2019 |
| 11 Dec 2018 | Other trial event | According to a Portola Pharmaceuticals media release, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has extended the review period for the Companys marketing authorization application (MAA) for Ondexxya (andexanet alfa), and cancelled the Oral Explanation scheduled for Wednesday, 12th Dec 2018. An opinion is now expected by 28th Feb 2019. Updated 24 Dec 2018 |
| 11 Dec 2018 | Other trial event | According to a Portola Pharmaceuticals media release, the CHMP informed Portola Pharmaceuticals that it will provide a list of outstanding questions related to the data package the Company submitted for Ondexxya last quarter, which will require additional responses from the Company. The preliminary timetable provided to the Company by the CHMP sets a deadline of 29th Jan 2019 for responses to the questions followed by a 30-day assessment period for the CHMP to review the Companys responses. Updated 24 Dec 2018 |
| 01 Oct 2018 | Biomarker Update | Biomarkers information updated Updated 07 Nov 2021 |
| 28 Sep 2018 | Other trial event | Last checked against ClinicalTrials.gov record. Updated 28 Sep 2018 |
| 29 Aug 2018 | Results | Results assessing reversal of apixaban and rivaroxaban anticoagulation by andexanet alfa in ANNEXA-A&R as assessed by non-tissue factor (TF)-initiated thrombin generation independent of TF pathway inhibitor, presented at the ESC Congress 2018: Annual Congress of the European Society of Cardiology Updated 14 Sep 2018 |
| 24 Jul 2018 | Results | Results (from ANNEXA-A, ANNEXA-R and ANNEXA-4) published in the American Journal of Medicine Updated 02 Aug 2018 |
| 03 May 2018 | Other trial event | Based on the results of ANNEXA-R, ANNEXA-A and interim data from ANNEXA-4, the Marketing Authorization Application (MAA) has been submitted to the European Medicines Agency (EMA) for andexanet alfa is under review. The Committee for Medicinal Products for Human Use (CHMP) communicated a positive trend vote on the MAA in February 2018. A formal opinion from the CHMP is expected by the end of 2018, and the European Commission is expected to issue a decision in early 2019. Updated 10 May 2018 |
| 03 May 2018 | Other trial event | According to a Portola Pharmaceuticals media release, based on the results of ANNEXA-R, ANNEXA-A and interim data from ANNEXA-4 (n=185), the U.S. Food and Drug Administration (FDA) has approved Andexxa, the first and only antidote for patients treated with rivaroxaban and apixaban, in reversing the anticoagulant activity of the Factor Xa inhibitors. Updated 10 May 2018 |
| 22 Dec 2017 | Other trial event | According to a Portola Pharmaceuticals media release, the U.S. Food and Drug Administration (FDA) will extend its review of the Biologics License Application (BLA) for AndexXa (andexanet alfa) by 90 days. The company recently submitted additional data requested by the agency for the ongoing ANNEXA-4 study as part of the continuing review process. The FDA communicated that the action date will move from February 3, 2018 to May 4, 2018. Updated 28 Dec 2017 |
| 15 Aug 2017 | Other trial event | According to a Portola Pharmaceuticals media release, the U.S. Food and Drug Administration (FDA) has found its resubmitted Biologics License Application (BLA) of AndexXa (andexanet alfa) to be acceptable for review, with an action due date of February 2, 2018. Updated 18 Aug 2017 |
| 03 Aug 2017 | Other trial event | According to a Portola Pharmaceuticals media release, the company resubmitted a Biologics License Application (BLA) to the Center for Biologics Evaluation and Research (CBER) of the U.S. FDA for of AndexXa (andexanet alfa). The resubmission includes supplemental information primarily related to manufacturing, as requested by the FDA in a complete response letter (CRL) issued to Portola in August 2016. Updated 10 Aug 2017 |
| 13 Oct 2016 | Other trial event | According to a Portola Pharmaceuticals media release, the company expects to resubmit a Biologics License Application (BLA), AndexXa in 2017. Updated 27 Oct 2016 |
| 19 Aug 2016 | Other trial event | According to a Portola Pharmaceuticals media release, based on data from this and other study (see profile 242840) Marketing Authorization Application (MAA) has been submitted to the European Medicines Agency (EMA), completed the validation period, and has been accepted for review. The MAA also included limited adjudicated efficacy and safety data from initial patients of ANNEXA-4 study. Updated 14 Sep 2016 |
| 17 Aug 2016 | Other trial event | According to a Portola Pharmaceuticals media release, company has received a Complete Response Letter (CRL) from the U.S. Food and Drug Administration (FDA) regarding its Biologics License Application (BLA) for AndexXa (andexanet alfa). Updated 12 Sep 2016 |
| 19 Feb 2016 | Results | Pooled analysis (n=298) of 3 trials [see ANNEXA-A, ANNEXA-R and CTP 700238713] were presented at the 41st International Stroke Conference. Updated 12 Apr 2016 |
| 17 Feb 2016 | Other trial event | According to a Portola Pharmaceuticals media release, the Center for Biologics Evaluation and Research (CBER) of the U.S FDA has accepted the Biologics License Application (BLA) for andexanet alfa for filing under a priority review. The FDA is expected to take action on the application by the Prescription Drug User Fee Act (PDUFA) action date of August 17, 2016. Updated 23 Feb 2016 |
| 01 Feb 2016 | Other trial event | According to Portola media release, the company plans to submit EU application of andexanet alfa in 2017. Updated 03 Feb 2016 |
| 18 Dec 2015 | Other trial event | According to Portola media release, submission of BLA to the US FDA was completed based upon the inputs from this trial. Updated 22 Dec 2015 |
| 11 Nov 2015 | Results | Results of ANNEXA-A and ANNEXA-R studies published in the New England Journal of Medicine Updated 18 Nov 2015 |
| 11 Nov 2015 | Results | According to a Portola Pharmaceuticals media release, pooled results of 2 studies including data from this trial and other study (see CTP 700242840) were published in The New England Journal of Medicine. Updated 18 Nov 2015 |
| 11 Nov 2015 | Results | Pooled results of 2 studies including data from this trial and other study (see CTP 700242840) were published in a Portola Pharmaceuticals media release. Updated 18 Nov 2015 |
| 01 Oct 2015 | Status change - completed | Status changed from recruiting to completed as reported by ClinicalTrials.gov. Updated 07 Oct 2015 |
| 04 Aug 2015 | Results | Data of this trial presented at the International Society on Thrombosis and haemostasis (ISTH) 2015, as per Portola Pharmaceutical media release. Updated 06 Aug 2015 |
| 22 Jun 2015 | Other trial event | According to a combined media release, full results from the second part of the study were presented at the International Society on Thrombosis and Haemostasis (ISTH) 2015 Congress. Updated 23 Jun 2015 |
| 22 Jun 2015 | Results | Results of part 2 of the trial published in the Media Release. Updated 23 Jun 2015 |
| 06 May 2015 | Other trial event | According to a Portola Pharmaceuticals media release, full results from the recently completed bolus plus infusion part of the study will be presented in an oral session at the International Society on Thrombosis and Haemostasis (ISTH) 2015 Congress. Updated 08 May 2015 |
| 08 Apr 2015 | Results | Positive results from the second part of ANNEXA-A study published in a Portola Pharmaceuticals media release. Updated 10 Apr 2015 |
| 08 Apr 2015 | Endpoint met | Primary endpoint (Reversal of Apixaban anticoagulation effect as measured by anti-factor Xa activity) has been met in the second part of the study, according to a Portola Pharmaceuticals media release. Updated 10 Apr 2015 |
| 12 Jan 2015 | Other trial event | According to a Portola Pharmaceuticals media release, the company plans to submit a Biologics Licence Application (BLA) to US FDA of Andexanet Alfa for the reversal of Factor Xa inhibitor anticoagulation in patients with major bleeding, by the end of 2015. The BLA will be submitted on the basis of this study and 2 other studies [see CTP 700248217 and 700242840]. Updated 04 Aug 2015 |
| 17 Nov 2014 | Results | Results from the first part of ANNEXA-A study presented at the 87th Annual Scientific Sessions of the American Heart Association. Updated 21 Jan 2015 |
| 17 Nov 2014 | Results | Positive results from the first part of ANNEXA-A study published in a Portola Pharmaceuticals media release. Updated 21 Jan 2015 |
| 01 Oct 2014 | Endpoint met | Primary endpoint (Reversal of Apixaban anticoagulation effect as measured by anti-factor Xa activity) has been met in the first part of the study, according to a Portola Pharmaceuticals media release. Updated 10 Apr 2015 |
| 01 Oct 2014 | Other trial event | Results show andexanet alfa has the potential to be the first agent approved as a universal Factor Xa inhibitor antidote; Portola Pharmaceuticals expects to file a BLA with the FDA for Accelerated Approval at the end of 2015, according to a media release. Updated 07 Oct 2014 |
| 01 Oct 2014 | Interim results | Top-line results published in Portola Pharmaceuticals media release. Updated 07 Oct 2014 |
| 14 Aug 2014 | Other trial event | New source identified and integrated (ClinicalTrials.gov; NCT02207725). Updated 14 Aug 2014 |
| 06 Aug 2014 | Other trial event | Portola Pharmaceuticals plans to report full data from ANNEXA-A and ANNEXA-R (see CT profile 700242840) studies in the first half of 2015. Updated 30 Sep 2014 |
| 19 Mar 2014 | Other trial event | Initial data from the trial is expected from the first part of the trial in the fourth quarter of 2014 according to a Portola Pharmaceuticals media release. Results from the second part of the trial is expected in early 2015. Updated 24 Mar 2014 |
| 19 Mar 2014 | Status change - recruiting | Status changed from planning to recruiting based on information reported in a Portola Pharmaceuticals media release. Updated 24 Mar 2014 |
| 19 Mar 2014 | Other trial event | Planned patient number (n=64) identified from a Portola Pharmaceuticals media release. Updated 24 Mar 2014 |
| 27 Feb 2014 | Other trial event | Portola Pharmaceuticals plans to report phase 3 data in the fourth quarter of 2014 and additional data in the first half of 2015. Updated 13 Aug 2014 |
| 03 Feb 2014 | Other trial event | Phase III trials are expected to begin in the first half of 2014 according to a Portola Pharmaceuticals media release. Updated 07 Apr 2014 |
| 18 Nov 2013 | New trial record | New trial record Updated 18 Nov 2013 |
Table of Contents
References
-
Portola Pharmaceuticals. Portola Pharmaceuticals Announces Phase 3 ANNEXA(TM)-A Study of Andexanet Alfa and Eliquis (Apixaban) Met Primary and Secondary Endpoints With High Statistical Significance. Media-Rel 2014;.
Media Release -
ClinicalTrials.gov: US National Institutes of Health. Trial-Reg 2023;.
Available from: URL: http://clinicaltrials.gov -
Portola Pharmaceuticals, Bristol-Myers Squibb, Pfizer. Portola, Bristol-Myers Squibb and Pfizer Announce Statistically Significant Results From the First Part of the Phase 3 ANNEXA(Tm)-A Studies of Investigational Andexanet Alfa With Eliquis (apixaban). Media-Rel 2014;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Announces Validation of Marketing Authorization Application (MAA) by European Medicines Agency (EMA) for IndexXa(TM) (andexanet alfa), a Factor Xa Inhibitor Antidote. Media-Rel 2016;.
Media Release -
Portola Pharmaceuticals. U.S. FDA Approves Portola Pharmaceuticals Andexxa(R), First and Only Antidote for the Reversal of Factor Xa Inhibitors. Media-Rel 2018;.
Media Release -
Bristol-Myers Squibb, Pfizer. Bristol-Myers Squibb and Pfizer Sign Collaboration with Portola Pharmaceuticals to Develop and Commercialize Investigational Andexanet Alfa in Japan. Media-Rel 2016;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Announces New Topline Data From Phase 3 ANNEXA-A(Tm) Trial Part 2: Breakthrough Designated Andexanet Alfa Successfully Meets Primary Endpoint for Prolonged Reversal of Factor Xa Inhibitor Eliquis (apixaban). Media-Rel 2015;.
Media Release -
Crowther M, Gold AM, Lu G, Leeds JM, Wiens BL, Mathur V, et al. Andexanet Alfa, a Universal Antidote for Reversal of Anticoagulation of Factor Xa Inhibitors in Healthy Human Volunteers. ISC-2016 2016; abstr. A212.
Available from: URL: http://stroke.ahajournals.org/content/47/Suppl_1/A212.abstract?sid=f62e60b5-7da6-4a2a-b286-4d2e500f47d547/Suppl_1/A212#cited-by -
Portola Pharmaceuticals. The New England Journal of Medicine Publishes Results of Portola Pharmaceuticals Phase 3 ANNEXA Studies of Andexanet Alfa. Media-Rel 2015;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Reports Fourth Quarter and Year-End 2013 Financial Results and Provides Corporate Update. Media-Rel 2014;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Supports World Thrombosis Day Campaign to Increase Awareness of Risks of Blood Clots. Media-Rel 2016;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Initiates Phase 4 Study to Support Accelerated Approval of Andexanet Alfa -- Its Breakthrough-Designated Factor Xa Inhibitor Antidote. Media-Rel 2015;.
Media Release -
Lu G, Lin J, Bronson M, Crowther M, Conley PB, Curnutte JT. Reversal of apixaban and rivaroxaban anticoagulation by andexanet alfa in ANNEXA-A&R as assessed by non-tissue factor (TF)-initiated thrombin generation independent of TF pathway inhibitor (TFPI). ESC-Card-2018 2018; abstr. 5069.
Available from: URL: http://link.adisinsight.com/w8PJo -
Portola Pharmaceuticals. Portola Pharmaceuticals Completes BLA Submission to U.S. Food and Drug Administration for Andexanet Alfa. Media-Rel 2015;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Announces AndexXa(R) (Andexanet Alfa) Biologics License Application Resubmission Accepted for Review by U.S. FDA. Media-Rel 2017;.
Media Release -
Portola Pharmaceuticals Inc. Portola Pharmaceuticals Announces Additional Positive Phase 2 Proof-of-Concept Data for Andexanet Alfa (PRT4445*). Media-Rel 2013;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Reports Second Quarter 2015 Financial Results and Provides Corporate Update. Media-Rel 2015;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Announces Resubmission of Biologics License Application for AndexXa(R) (Andexanet Alfa). Media-Rel 2017;.
Media Release -
Siegal DM, Curnutte JT, Connolly SJ, Lu G, Conley PB, Wiens BL, et al. Andexanet Alfa for the Reversal of Factor Xa Inhibitor Activity. N-Engl-J-Med 2015;.
PubMed | CrossRef Fulltext -
Rogers KC, Finks SW. A New Option for Reversing the Anticoagulant Effect of Factor Xa Inhibitors: Andexanet alfa (Andexxa(R)). Am-J-Med 2018;.
PubMed | CrossRef Fulltext -
Portola Pharmaceuticals. Portola Pharmaceuticals Announces Biologics License Application for Andexanet Alfa Accepted for Review by FDA. Media-Rel 2016;.
Media Release -
Momin JH, Hughes GJ. Andexanet alfa (Andexxa) for the reversal of direct oral anticoagulants. PT 2019;44(9):530-549.
PubMed | CrossRef Fulltext -
Portola Pharmaceuticals. European CHMP Adopts Positive Opinion on Ondexxya(T) (andexanet alfa) Portola Pharmaceuticals Factor Xa Inhibitor Reversal Agent. Media-Rel 2019;.
Media Release -
Portola Pharmaceuticals. Portola Pharmaceuticals Initiates Phase 3 Study of Andexanet Alfa, Potential First-in-Class Factor Xa Inhibitor Reversal Agent, Under Accelerated Approval Pathway. Media-Rel 2014;.
Media Release -
Crowther M, Levy GG, Lu G, Leeds J, Barron L, Conley PB, et al. ANNEXA(TM)-A: A Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial, Demonstrating Reversal of Apixaban-Induced Anticoagulation in Older Subjects by Andexanet alfa (PRT064445), a Universal Antidote for Factor Xa (fXa) Inhibitors. AHA-2014 2014; abstr. N/A.
Available from: URL: http://link.adisinsight.com/Yt8z5 -
Portola Pharmaceuticals. Portola Pharmaceuticals Receives Complete Response Letter from FDA for Biologics License Application for AndexXa(TM) (andexanet alfa). Media-Rel 2016;.
Media Release -
Portola Pharmaceuticals. CHMP Extends Review Period for Portola Pharmaceuticals Ondexxya(Tm) (andexanet alfa). Media-Rel 2018;.
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Portola Pharmaceuticals. European Commission Grants Conditional Marketing Authorization for Portola Pharmaceuticals' Ondexxya(Tm) (andexanet alfa), the First and Only Antidote for the Reversal of Factor Xa Inhibitors. Media-Rel 2019;.
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Portola Pharmaceuticals. Portola Pharmaceuticals Provides Update on Biologics License Application (BLA) for AndexXa(R) (andexanet alfa). Media-Rel 2017;.
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Portola Pharmaceuticals. Portola Pharmaceuticals Enters Into Clinical Collaboration Agreement With Bayer and Janssen for Phase 3 Studies of Andexanet Alfa*, Investigational Factor Xa Inhibitor Reversal Agent, and XARELTO(Rm). Media-Rel 2014;.
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Portola Pharmaceuticals. Portola Pharmaceuticals Reports Second Quarter Financial Results and Provides Corporate Update. Media-Rel 2014;.
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Portola Pharmaceuticals, Bristol-Meyers Squibb, Pfizer. Portola, Bristol-Myers Squibb and Pfizer Announce Full Results of Second Part of Phase 3 ANNEXA-A(Tm) Study Demonstrating That Investigational Andexanet Alfa Sustained Reversal of Anticoagulant Effect of Factor Xa Inhibitor Eliquis (apixaban). Media-Rel 2015;.
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Portola Pharmaceuticals. Portola Pharmaceuticals Reports First Quarter 2015 Financial Results and Provides Corporate Update. Media-Rel 2015;.
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Portola Pharmaceuticals. Portola Pharmaceuticals Announces Commercial Supply Agreement for Andexanet Alfa With Lonza. Media-Rel 2014;.
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