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  1. pharmadog
  2. ›drugs
  3. ›Eliquis
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apixaban ODT

Marketedupdated 4mo ago
by Bristol-Myers Squibb Co
Approved
annual revenue · 2024–2024peak $13.3B
2024: $13.3B2024$13.3B
community read0 votes

🐶 often sniffed alongside

top 8
  • drugapixaban5 co-mentions · 2 sources
  • drugapixaban ER5 co-mentions · 2 sources
  • tagOncology2 co-mentions · 1 sources
  • tagHematology2 co-mentions · 1 sources
  • tagAdCom2 co-mentions · 1 sources
  • tag510(k) Clearance2 co-mentions · 1 sources
  • tagDiagnostics Company2 co-mentions · 1 sources
  • companyMedical University of Gdansk1 co-mentions · 1 sources

Small molecule drug with a maximum clinical stage of Approval (across all indications), with 8 approved and 14 investigational indications.

all catalysts(1)

phase 2 completion · 1
Apr 30, 2026
phase 2 completion
4mo ago
Medical University of Gdansk — apixaban (Phase II Trial Completion)
apixaban ODT
→

Trials studying apixaban ODT

  • phase2Safety in Adult Participants With Atrial Fibrillation Who Are Treated With Anticoagulationrecruitingn=1,200
  • phase3Treatment and Secondary Prevention of Venous Thromboembolism (VTE) in Adult Participants With Solid and Hematologic Cancersrecruitingn=1,600
  • phase3A Study of Milvexian Versus Apixaban in Participants With Atrial Fibrillationactive not recruitingn=20,284
  • N/ADEFIANCE: RCT of ClotTriever System Versus Anticoagulation In Deep Vein Thrombosisrecruitingn=300
  • phase1A Study to Investigate Andexanet Dosing and the Interaction Between Andexanet and Subsequent Enoxaparin in Healthy Participantsrecruitingn=186
  • phase3REGN7508 Versus Apixaban and Enoxaparin for Thromboprophylaxis After Total Knee Arthroplasty in Adultsrecruitingn=2,000
  • —Anticoagulation in Patients With Venous Thromboembolism and Canceractive not recruitingn=1
  • —High Gastrointestinal Bleed Risk Outcomes in Patients With Non-valvular Atrial Fibrillation (NVAF) in Franceactive not recruitingn=1
more trials →

Patent cliff

source: FDA Orange Book
first barrier falls
Nov 21, 2026
87 days

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (16)

  • May 22, 2041patentUS 11896586*PED
  • Nov 22, 2040formulationUS 11896586
  • Aug 24, 2031patentUS 9326945*PED5.0y
  • Aug 24, 2031patentUS 9326945*PED5.0y
  • Aug 24, 2031patentUS 9326945*PED5.0y
  • Feb 24, 2031formulationUS 93269454.5y
  • Feb 24, 2031formulationUS 93269454.5y
  • Feb 24, 2031formulationUS 93269454.5y
  • May 21, 2027patentUS 6967208*PED268d
  • May 21, 2027patentUS 6967208*PED268d
  • May 21, 2027patentUS 6967208*PED268d
  • May 21, 2027patentUS 6967208*PED268d
  • Nov 21, 2026compositionUS 696720887d
  • Nov 21, 2026compositionUS 696720887d
  • Nov 21, 2026compositionUS 696720887d
  • Nov 21, 2026compositionUS 696720887d

FDA exclusivities (8)

  • Oct 17, 2028PEDPediatric (6mo bonus)2.1y
  • Oct 17, 2028PEDPediatric (6mo bonus)2.1y
  • Oct 17, 2028PEDPediatric (6mo bonus)2.1y
  • Oct 17, 2028PEDPediatric (6mo bonus)2.1y
  • Apr 17, 2028NPPNew Product (3y)1.6y
  • Apr 17, 2028NPPNew Product (3y)1.6y
  • Apr 17, 2028NSNS1.6y
  • Apr 17, 2028NPNP1.6y

News(10)

  • BMS picks Texas for new $2.3B manufacturing campus
    Bristol Myers Squibb’s $2.3 billion Houston manufacturing campus is part of the company’s larger $40 billion investment designed to bolster American innovation and manufacturing.
    biospace · 15d ago
  • Earnings roundup: Gilead’s ‘uncertain’ future, Pfizer’s crossroads and Merck’s PCSK9 launch
    Some analysts see warning signs in crucial drug launches from Gilead and Merck, while an important trial readout could change Pfizer’s growth trajectory.
    biopharma_dive · 20d ago
  • No deal between AstraZeneca and BMS, senior source insists: Reuters
    Reuters has deflated rumors that AstraZeneca and Bristol Myers Squibb are discussing a possible merger, letting the air out of industry-wide speculation over what could have been the largest deal i…
    biospace · 20d ago
  • Rumors of biggest pharma merger ever drop amid Q2 earnings, contentious FDA adcomms
    The industry has been abuzz since the weekend when talks of a potential mega-merger between Bristol Myers Squibb and AstraZeneca were reported. Meanwhile, Pfizer, Merck and others release second qu…
    biospace · 20d ago
  • Pfizer CEO defends $7B bolt-on M&A strategy as peers rush to buy
    Asked on a second quarter earnings call if Pfizer could direct more money to M&A amid a feeding frenzy across the pharma industry, CEO Albert Bourla defended his strategy.
    biospace · 21d ago
  • Pfizer expands multibillion-dollar cost-cutting plan
    Hatched three years ago, the restructuring is now expected to deliver $1 billion in new cost reductions and save Pfizer another $1.5 billion by streamlining drug production.
    biopharma_dive · 21d ago
  • As portfolio erodes, BMS stands to gain a lot from rumored AstraZeneca merger
    While both drugmakers face looming patent cliffs, analysts say joining forces could help Bristol Myers Squibb replenish its eroding portfolio—while the strategic case for AstraZeneca seems to be mo…
    biospace · 21d ago
  • Pfizer cuts $2.5B more across R&D, manufacturing in ongoing restructure
    The additional cuts, which will primarily occur between 2027 and 2029, will cost some $6 billion as the pharma tries to ride out a post-COVID headache while facing stiff patent headwinds for major…
    biospace · 21d ago
  • An AstraZeneca-Bristol Myers megamerger? Wall Street isn’t thrilled.
    In fact, the former lost tens of billions of dollars in market value following reports of a potential tie-up between the pharmaceutical giants.
    biopharma_dive · 22d ago
  • Editor’s Corner: Why an AstraZeneca-Bristol Myers Squibb merger is a bad idea
    Combining the two drugmakers would trigger severe regulatory concerns and significant pipeline disruptions, cost numerous jobs, all while damaging the broader biopharma ecosystem and hurting patien…
    fiercebiotech · 23d ago
view all news mentions →
brand
Eliquis
generic
apixaban
MOA
Coagulation factor X inhibitor
indication
Venous Thromboembolism
phase
marketed
approved
2012-12-28
Data sources
openFDA · ClinicalTrials.gov
last refreshed 49m ago
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