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 →
Sign InSubscribe
pharmadog

fetch the data · sniff the signal

Discover
  • Jobs
  • News
Hubs
  • Topics
  • Patent cliff
  • Publications
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. ›LINAGLIPTIN
drug
save

LINAGLIPTIN

Marketedupdated 3mo ago
by Boehringer Ingelheim Corp
Approved
community read0 votes

🐶 often sniffed alongside

top 8
  • tagApproval24 co-mentions · 8 sources
  • drugLINAGLIPTIN AND METFORMIN HYDROCHLORIDE20 co-mentions · 8 sources
  • tagSmall Molecule12 co-mentions · 8 sources
  • drugSITAGLIPTIN AND METFORMIN HYDROCHLORIDE8 co-mentions · 4 sources
  • drugmetformin8 co-mentions · 4 sources
  • drugmetformin hydrochloride8 co-mentions · 4 sources
  • drugmetformin hydrochloride ER8 co-mentions · 4 sources
  • drugmetformin hydrochloride SR8 co-mentions · 4 sources

indications

investigational
Type 2 Diabetes

all catalysts(4)

approval · 4
Nov 3, 2025
approval
10mo ago
LINAGLIPTIN AND METFORMIN HYDROCHLORIDE (LINAGLIPTIN) — FDA approval
LINAGLIPTIN
→
Nov 3, 2025
approval
10mo ago
LINAGLIPTIN — FDA approval
LINAGLIPTIN
→
Nov 3, 2025
approval
10mo ago
LINAGLIPTIN — FDA approval
LINAGLIPTIN
→
Nov 3, 2025
approval
10mo ago
LINAGLIPTIN — FDA approval
LINAGLIPTIN
→

Trials studying LINAGLIPTIN

  • phase4Glycemic Control With Triple Pathway Approach Through Empagliflozin, Linagliptin and Metformin Combinationrecruitingn=800
  • phase4Glycemic Variability of Combination Therapies in T2DMrecruitingn=178
  • phase2A Study of Multiple Immunotherapy-Based Treatment Combinations in Patients With Locally Advanced Unresectable or Metastatic Gastric or Gastroesophageal Junction Cancer (G/GEJ) or Esophageal Cancer (Morpheus-Gastric and Esophageal Cancer)completedn=214
  • phase2A Study Of Multiple Immunotherapy-Based Treatment Combinations In Participants With Metastatic Non-Small Cell Lung Cancer (Morpheus- Non-Small Cell Lung Cancer)completedn=314
  • phase3Efficacy and Safety of Madalena Association in the Treatment of Type II Diabetes Mellitusrecruitingn=270
  • phase1Bioequivalence Study to Compare Empagliflozin/Linagliptin/Metformin HCL 25mg/5mg/1000mg Extended-Release Tablets Versus Trijardy® XR Extended Release Film Coated Tabletscompletedn=14
  • —Esgliteo Post Marketing Surveillance (PMS) in Korean Patients With Type 2 Diabetes Mellituscompletedn=1,053
  • phase1To Compare and Evaluate the Oral Bioavailability of Empagliflozin + Linagliptin 10 mg/5 mg Filmcoated Tablets With That of Glyxambi 10 mg/ 5 mg Film-coated Tablets in Healthy, Adult, Human Subjects Under Fasting Conditions.completedn=40
more trials →

Patent cliff

source: FDA Orange Book
first barrier falls
Dec 20, 2026
127 days

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

patents (63)

  • 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
  • Sep 5, 2031patentUS 8853156*PED
  • Mar 5, 2031formulationUS 88531564.6y
  • Dec 4, 2030patentUS 8846695*PED4.3y
  • Dec 4, 2030patentUS 8846695*PED4.3y
  • Dec 4, 2030patentUS 8846695*PED4.3y
  • Dec 4, 2030patentUS 8846695*PED4.3y
  • Nov 21, 2030patentUS 9155705*PED4.3y
  • Nov 21, 2030patentUS 9155705*PED4.3y
  • Nov 21, 2030patentUS 9155705*PED4.3y
  • Jun 4, 2030method-of-use (U-1503)US 88466953.8y
  • Jun 4, 2030method-of-use (U-1503)US 88466953.8y
  • May 21, 2030formulationUS 91557053.8y
  • May 21, 2030formulationUS 91557053.8y
  • May 21, 2030formulationUS 91557053.8y
  • Apr 10, 2030method-of-use (U-3854)US 119113883.7y
  • Apr 10, 2030method-of-use (U-3854)US 119113883.7y
  • Apr 10, 2030method-of-use (U-3854)US 119113883.7y
  • Apr 10, 2030method-of-use (U-3854)US 119113883.7y
  • Feb 5, 2030patentUS 10034877*PED3.5y
  • Feb 5, 2030patentUS 9486526*PED3.5y
  • Oct 2, 2029patentUS 10022379*PED3.1y
  • Oct 2, 2029patentUS 10022379*PED3.1y
  • Oct 2, 2029patentUS 10022379*PED3.1y
  • Oct 2, 2029patentUS 10973827*PED3.1y
  • Oct 2, 2029patentUS 10973827*PED3.1y
  • Oct 2, 2029patentUS 10973827*PED3.1y
  • Oct 2, 2029patentUS 9415016*PED3.1y
  • Oct 2, 2029patentUS 9415016*PED3.1y
  • Oct 2, 2029patentUS 9415016*PED3.1y
  • Aug 5, 2029method-of-use (U-2347)US 100348773.0y
  • Aug 5, 2029method-of-use (U-1915)US 94865263.0y
  • Apr 2, 2029method-of-use (U-2339)US 100223792.6y
  • Apr 2, 2029method-of-use (U-2339)US 100223792.6y
  • Apr 2, 2029method-of-use (U-2339)US 100223792.6y
  • Apr 2, 2029formulationUS 109738272.6y
  • Apr 2, 2029formulationUS 109738272.6y
  • Apr 2, 2029formulationUS 109738272.6y
  • Apr 2, 2029formulationUS 94150162.6y
  • Apr 2, 2029formulationUS 94150162.6y
  • Apr 2, 2029formulationUS 94150162.6y
  • Nov 4, 2027patentUS 11033552*PED1.2y
  • Nov 4, 2027patentUS 8673927*PED1.2y
  • Nov 4, 2027patentUS 8673927*PED1.2y
  • Nov 4, 2027patentUS 8673927*PED1.2y
  • Nov 4, 2027patentUS 8673927*PED1.2y
  • May 4, 2027formulationUS 11033552262d
  • May 4, 2027formulationUS 12178819262d
  • 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

FDA exclusivities (8)

  • Dec 20, 2026PEDPediatric (6mo bonus)127d
  • Dec 20, 2026PEDPediatric (6mo bonus)127d
  • Dec 20, 2026PEDPediatric (6mo bonus)127d
  • Dec 20, 2026PEDPediatric (6mo bonus)127d
  • Jun 20, 2026M-295Method (3y)
  • Jun 20, 2026M-295Method (3y)
  • Jun 20, 2026M-295Method (3y)
  • Jun 20, 2026M-295Method (3y)

News(0)

no news has mentioned this drug yet

brand
LINAGLIPTIN
generic
LINAGLIPTIN
indication
Type 2 Diabetes
phase
marketed
Data sources
openFDA · ClinicalTrials.gov
last refreshed 28m 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?