Evidence map›Paper›PMID 29296829›Full record

ArticleBlood advances2017

Safety, pharmacokinetics, and reversal of apixaban anticoagulation with andexanet alfa.

Deborah Siegal, Genmin Lu, Janet M Leeds, Mark Karbarz, Janice Castillo, Vandana Mathur, Athiwat Hutchaleelaha, Uma Sinha, Michael Kitt, Matt McClure and 4 more

Abstract read
In one paragraph

Article in Blood advances, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Andexanet alfa for the reversal of the low-molecular-weight heparin enoxaparin.Research and practice in thrombosis and haemostasis · 2025
    Article
  10. Observational
  11. Article
  12. Andexanet alfa: trials just leave us with more questions.Research and practice in thrombosis and haemostasis · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Andexanet Alfa (AndexxaP & T : a peer-reviewed journal for formulary management · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Deborah SiegalDepartment of Medicine, McMaster University, Hamilton, ON, Canada.
Genmin LuPortola Pharmaceuticals, San Francisco, CA; and.
Janet M LeedsPortola Pharmaceuticals, San Francisco, CA; and.
Mark KarbarzPortola Pharmaceuticals, San Francisco, CA; and.
Janice CastilloPortola Pharmaceuticals, San Francisco, CA; and.
Vandana MathurMathur Consulting, San Francisco, CA.
Athiwat HutchaleelahaPortola Pharmaceuticals, San Francisco, CA; and.
Uma SinhaPortola Pharmaceuticals, San Francisco, CA; and.
Michael KittPortola Pharmaceuticals, San Francisco, CA; and.
Matt McClurePortola Pharmaceuticals, San Francisco, CA; and.
Stanley J HollenbachPortola Pharmaceuticals, San Francisco, CA; and.
John T CurnuttePortola Pharmaceuticals, San Francisco, CA; and.
Pamela B ConleyPortola Pharmaceuticals, San Francisco, CA; and.
Mark CrowtherDepartment of Medicine, McMaster University, Hamilton, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Direct factor Xa (FXa) inhibitors lack a specific reversal agent for emergencies such as major bleeding or urgent surgery. Andexanet alfa, a modified, catalytically inactive, recombinant human FXa derivative, reverses anticoagulant effect by binding and sequestering FXa inhibitors. This original report of safety and dose-finding, phase 1 and 2 randomized, double-blind, placebo-controlled studies, investigated various doses of andexanet in healthy volunteers. Phase 1 evaluated the safety and pharmacokinetics of andexanet (n = 24) or placebo (n = 8). In phase 2, andexanet (n = 36) or placebo (n = 18) was administered following steady-state apixaban dosing (5 mg twice daily for 6 days); safety, pharmacokinetics, and pharmacodynamics were assessed. Andexanet plasma concentration increased proportionally with dose, with rapid elimination (terminal elimination half-life, 4.35-7.5 hours). Following apixaban treatment, andexanet rapidly (≤2 minutes) and dose dependently reduced unbound apixaban concentration vs placebo (51% to 89% vs 5% reduction; all

Identifiers

PMID29296829
PMCPMC5728098

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.