pharmadog
News
when
  • Latest
  • Archive
by source
  • All Sources
  • Sources Page
Jobs
department
  • Clinical
  • Regulatory
  • Medical Affairs
  • Commercial
  • R&D / Discovery
  • Biostatistics / Data
  • Manufacturing / CMC
  • Market Access
therapeutic area
  • Oncology
  • Immunology
  • Neuroscience
  • Cardiovascular
  • Metabolic
  • Rare Disease
  • Infectious Disease
location & type
  • Remote Only
  • US Only
  • California
  • Massachusetts
  • Internships
  • Phase 3 Roles
  • All Jobs →
Drugs
by stage
  • Marketed
  • Phase 3
  • Phase 2
  • Phase 1
  • Preclinical
browse
  • Most catalysts
  • Recently active
  • All drugs →
  • Companies
  • Patent cliff
Calendar
what
  • Trial readouts
  • PDUFA dates
  • Approvals
  • Earnings
when
  • Upcoming
  • Month grid
  • Recently passed
Sign InSubscribe
pharmadog

fetch the data · sniff the signal

Discover
  • Jobs
  • News
  • Drugs
  • Calendar
  • Companies
Hubs
  • Topics
  • Patent cliff
  • Publications
  • Readouts
Tools
  • Compare
  • Search
  • Bookmarks
Trust
  • About
  • Sources
  • Contact
Legal
  • Privacy
  • Terms
  • Pricing

© 2026 pharmadog.xyz

made by humans and a good dog

  • home
  • jobs
  • news
  • search
  1. pharmadog
  2. ›drugs
  3. ›Trijardy XR
drug
save

(empagliflozin + linagliptin + metformin hydrochloride) ER

Marketedupdated 5mo ago
by Boehringer Ingelheim Corp
Approved
community read0 votes

🐶 often sniffed alongside

top 4
  • drugTRIJARDY XR14 co-mentions · 7 sources
  • tagApproval14 co-mentions · 7 sources
  • companyBoehringer Ingelheim Corp7 co-mentions · 7 sources
  • tagSmall Molecule7 co-mentions · 7 sources

indications

investigational
Type 2 Diabetes

all catalysts(7)

approval · 7
Jan 27, 2020
approval
7y ago
TRIJARDY XR (EMPAGLIFLOZIN) — FDA approval
(empagliflozin + linagliptin + metformin hydrochloride) ER
→
Oct 30, 2020
approval
6y ago
TRIJARDY XR (EMPAGLIFLOZIN) — FDA approval
(empagliflozin + linagliptin + metformin hydrochloride) ER
→
Jun 11, 2021
approval
5y ago
TRIJARDY XR (EMPAGLIFLOZIN) — FDA approval
(empagliflozin + linagliptin + metformin hydrochloride) ER
→
Jun 11, 2021
approval
5y ago
TRIJARDY XR (EMPAGLIFLOZIN) — FDA approval
(empagliflozin + linagliptin + metformin hydrochloride) ER
→
Oct 13, 2022
approval
4y ago
TRIJARDY XR (EMPAGLIFLOZIN) — FDA approval
(empagliflozin + linagliptin + metformin hydrochloride) ER
→
Oct 30, 2023
approval
3y ago
TRIJARDY XR (EMPAGLIFLOZIN) — FDA approval
(empagliflozin + linagliptin + metformin hydrochloride) ER
→
Oct 24, 2025
approval
12mo ago
TRIJARDY XR (EMPAGLIFLOZIN) — FDA approval
(empagliflozin + linagliptin + metformin hydrochloride) ER
→

Patent cliff

source: FDA Orange Book
first barrier falls
Apr 15, 2027
193 days

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

patents (103)

  • Dec 8, 2037patentUS 12364700*PED
  • Dec 8, 2037patentUS 12364700*PED
  • Dec 8, 2037patentUS 12364700*PED
  • Dec 8, 2037patentUS 12364700*PED
  • Jun 8, 2037method-of-use (U-4224)US 12364700
  • Jun 8, 2037method-of-use (U-4224)US 12364700
  • Jun 8, 2037method-of-use (U-4224)US 12364700
  • Jun 8, 2037method-of-use (U-4224)US 12364700
  • Dec 11, 2034patentUS 9949998*PED
  • Dec 11, 2034patentUS 9949998*PED
  • Dec 11, 2034patentUS 9949998*PED
  • Dec 11, 2034patentUS 9949998*PED
  • Oct 3, 2034patentUS 10258637*PED
  • Oct 3, 2034patentUS 10258637*PED
  • Oct 3, 2034patentUS 10258637*PED
  • Oct 3, 2034patentUS 10258637*PED
  • Oct 3, 2034patentUS 11090323*PED
  • Oct 3, 2034patentUS 11090323*PED
  • Oct 3, 2034patentUS 11090323*PED
  • Oct 3, 2034patentUS 11090323*PED
  • Oct 3, 2034patentUS 11833166*PED
  • Oct 3, 2034patentUS 11833166*PED
  • Oct 3, 2034patentUS 11833166*PED
  • Oct 3, 2034patentUS 11833166*PED
  • Jun 11, 2034method-of-use (U-2731)US 9949998
  • Jun 11, 2034method-of-use (U-2731)US 9949998
  • Jun 11, 2034method-of-use (U-2731)US 9949998
  • Jun 11, 2034method-of-use (U-2731)US 9949998
  • Apr 3, 2034method-of-use (U-2731)US 10258637
  • Apr 3, 2034method-of-use (U-2731)US 10258637
  • Apr 3, 2034method-of-use (U-2731)US 10258637
  • Apr 3, 2034method-of-use (U-2731)US 10258637
  • Apr 3, 2034method-of-use (U-3192)US 11090323
  • Apr 3, 2034method-of-use (U-3192)US 11090323
  • Apr 3, 2034method-of-use (U-3192)US 11090323
  • Apr 3, 2034method-of-use (U-3192)US 11090323
  • Apr 3, 2034method-of-use (U-3777)US 11833166
  • Apr 3, 2034method-of-use (U-3777)US 11833166
  • Apr 3, 2034method-of-use (U-3777)US 11833166
  • Apr 3, 2034method-of-use (U-3777)US 11833166
  • Mar 7, 2032formulationUS 10596120
  • Mar 7, 2032formulationUS 10596120
  • Mar 7, 2032formulationUS 10596120
  • Mar 7, 2032formulationUS 10596120
  • Mar 7, 2032formulationUS 11564886
  • Mar 7, 2032formulationUS 11564886
  • Mar 7, 2032formulationUS 11564886
  • Aug 11, 2030patentUS 12115179*PED3.9y
  • Aug 11, 2030patentUS 12115179*PED3.9y
  • Aug 11, 2030patentUS 12115179*PED3.9y
  • Aug 11, 2030patentUS 12115179*PED3.9y
  • Jun 15, 2030formulationUS 104061723.7y
  • Jun 15, 2030formulationUS 104061723.7y
  • Jun 15, 2030formulationUS 104061723.7y
  • Jun 15, 2030formulationUS 104061723.7y
  • May 21, 2030formulationUS 91557053.6y
  • May 21, 2030formulationUS 91557053.6y
  • May 21, 2030formulationUS 91557053.6y
  • May 21, 2030formulationUS 91557053.6y
  • Apr 14, 2030patentUS 8551957*PED3.5y
  • Apr 14, 2030patentUS 8551957*PED3.5y
  • Apr 14, 2030patentUS 8551957*PED3.5y
  • Apr 14, 2030patentUS 8551957*PED3.5y
  • Feb 11, 2030method-of-use (U-4023)US 121151793.4y
  • Feb 11, 2030method-of-use (U-4023)US 121151793.4y
  • Feb 11, 2030method-of-use (U-4023)US 121151793.4y
  • Feb 11, 2030method-of-use (U-4023)US 121151793.4y
  • Oct 14, 2029formulationUS 85519573.0y
  • Oct 14, 2029formulationUS 85519573.0y
  • Oct 14, 2029formulationUS 85519573.0y
  • Oct 14, 2029formulationUS 85519573.0y
  • Apr 2, 2029formulationUS 100223792.5y
  • Apr 2, 2029formulationUS 100223792.5y
  • Apr 2, 2029formulationUS 100223792.5y
  • Apr 2, 2029formulationUS 100223792.5y
  • Apr 2, 2029formulationUS 94150162.5y
  • Apr 2, 2029formulationUS 94150162.5y
  • Apr 2, 2029formulationUS 94150162.5y
  • Apr 2, 2029formulationUS 94150162.5y
  • Feb 1, 2029patentUS 7579449*PED2.3y
  • Feb 1, 2029patentUS 7579449*PED2.3y
  • Feb 1, 2029patentUS 7579449*PED2.3y
  • Feb 1, 2029patentUS 7579449*PED2.3y
  • Aug 1, 2028compositionUS 75794491.8y
  • Aug 1, 2028compositionUS 75794491.8y
  • Aug 1, 2028compositionUS 75794491.8y
  • Aug 1, 2028compositionUS 75794491.8y
  • Oct 15, 2027patentUS 7713938*PED1.0y
  • Oct 15, 2027patentUS 7713938*PED1.0y
  • Oct 15, 2027patentUS 7713938*PED1.0y
  • Oct 15, 2027patentUS 7713938*PED1.0y
  • Apr 15, 2027compositionUS 7713938193d
  • Apr 15, 2027compositionUS 7713938193d
  • Apr 15, 2027compositionUS 7713938193d
  • Apr 15, 2027compositionUS 7713938193d
  • May 26, 2026patentUS 8883805*PED
  • May 26, 2026patentUS 8883805*PED
  • May 26, 2026patentUS 8883805*PED
  • May 26, 2026patentUS 8883805*PED
  • Nov 26, 2025formulationUS 8883805
  • Nov 26, 2025formulationUS 8883805
  • Nov 26, 2025formulationUS 8883805
  • Nov 26, 2025formulationUS 8883805

News(0)

no news has mentioned this drug yet

brand
Trijardy XR
generic
(empagliflozin + linagliptin + metformin hydrochloride)
indication
Type 2 Diabetes
phase
marketed
Data sources
openFDA · ClinicalTrials.gov
last refreshed 27m ago
Found something off?
🐶 something off?

Report a data issue

Tell Bork what looks wrong — wrong sponsor, stale phase, mislinked ticker, anything. We’ll triage and fix.

comments(0)

5-min edit window · permanent after that
sign in to leave a comment · permanent archive after 5 minutes
no comments yet — first sniff?