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  1. pharmadog
  2. ›drugs
  3. ›ZEPBOUND
drug · protein
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ZEPBOUND

Marketedupdated 5mo ago
/ tur-ZEP-ə-tyde /
by $LLY ELI LILLY & Co🔗 ChEMBL
Approved
annual revenue · 2024–2024peak $4.9B
2024: $4.9B2024$4.9B
community read0 votes

🐶 often sniffed alongside

top 6
  • drugMOUNJARO112 co-mentions · 40 sources
  • drugtirzepatide112 co-mentions · 40 sources
  • tagApproval96 co-mentions · 24 sources
  • companyEli Lilly and Co48 co-mentions · 24 sources
  • tagRecall16 co-mentions · 16 sources
  • drugcyanocobalamin2 co-mentions · 2 sources

Protein drug with a maximum clinical stage of Approval (across all indications), with 6 approved and 8 investigational indications.

indications

investigational
Obesity

targets

Glucagon-like peptide 1 receptorGastric inhibitory polypeptide receptor

all catalysts(24)

approval · 24
May 13, 2022
approval
$LLY1142.85-0.61%
4y ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Jul 28, 2023
approval
$LLY1142.85-0.61%
3y ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Jul 28, 2023
approval
$LLY1142.85-0.61%
3y ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Nov 8, 2023
approval
$LLY1142.85-0.61%
3y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Mar 28, 2024
approval
$LLY1142.85-0.61%
3y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Oct 18, 2024
approval
$LLY1142.85-0.61%
2y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Oct 18, 2024
approval
$LLY1142.85-0.61%
2y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Oct 18, 2024
approval
$LLY1142.85-0.61%
2y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Oct 18, 2024
approval
$LLY1142.85-0.61%
2y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Oct 18, 2024
approval
$LLY1142.85-0.61%
2y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Nov 1, 2024
approval
$LLY1142.85-0.61%
2y ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Nov 1, 2024
approval
$LLY1142.85-0.61%
2y ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Nov 1, 2024
approval
$LLY1142.85-0.61%
2y ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Dec 20, 2024
approval
$LLY1142.85-0.61%
2y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Feb 7, 2025
approval
$LLY1142.85-0.61%
2y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
May 28, 2025
approval
$LLY1142.85-0.61%
1y ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Sep 25, 2025
approval
$LLY1142.85-0.61%
1y ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Sep 25, 2025
approval
$LLY1142.85-0.61%
1y ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Dec 19, 2025
approval
$LLY1142.85-0.61%
10mo ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Jan 7, 2026
approval
$LLY1142.85-0.61%
9mo ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Jan 7, 2026
approval
$LLY1142.85-0.61%
9mo ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Jan 20, 2026
approval
$LLY1142.85-0.61%
9mo ago
MOUNJARO (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Jan 20, 2026
approval
$LLY1142.85-0.61%
9mo ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
Feb 25, 2026
approval
$LLY1142.85-0.61%
7mo ago
ZEPBOUND (TIRZEPATIDE) — FDA approval
ZEPBOUND
→
view all 24 catalysts →

Trials studying ZEPBOUND

  • phase3Efficacy, Safety, and Pharmacokinetics of Tirzepatide (LY3298176) Once Weekly Versus Placebo in Pediatric Participants 6 to Less Than 12 Years of Age Who Have Obesity (ADVANCE-SURMOUNT-KIDS)not yet recruitingn=150
  • phase2Efficacy and Safety of Tirzepatide Versus Placebo or Lisdexamfetamine Dimesylate for Binge-Eating Disorderrecruitingn=105
  • phase3A Study of Tirzepatide in Adolescents With Obesity and Weight-Related Comorbidities (SURMOUNT-ADOLESCENTS-2)recruitingn=300
  • phase3A Research Study to See How Much CagriSema Lowers Blood Sugar and Body Weight Compared to Tirzepatide in People With Type 2 Diabetes Treated With Metformin With or Without an SGLT2 Inhibitorcompletedn=1,024
  • phase4Bariatric Surgery vs. Semaglutide vs. Tirzepatideactive not recruitingn=140
  • phase2A Study of SYH2069 Injection in Participants With T2DM Not Controlled With Diet/Exercise Alone or Metforminnot yet recruitingn=240
  • phase3Mirikizumab and Tirzepatide Administered in Adult Participants With Moderately to Severely Active Crohn's Disease and Obesity or Overweightrecruitingn=290
  • phase2A Study to Evaluate ALN-2232 in Participants With Obesityrecruitingn=156

Patent cliff

source: FDA Orange Book
first barrier falls
Nov 8, 2026
34 days

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

patents (216)

  • Dec 30, 2041method-of-use (U-4193)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4193)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4193)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4193)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4192)US 12295987
  • Dec 30, 2041method-of-use (U-4193)US 12295987
  • Dec 30, 2041method-of-use (U-4193)US 12295987
  • Dec 30, 2041method-of-use (U-4193)US 12295987
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4232)US 12343382
  • Jul 22, 2039method-of-use (U-4232)US 12343382
  • Jul 22, 2039method-of-use (U-4232)US 12343382
  • Jul 22, 2039method-of-use (U-4232)US 12343382
  • Jul 22, 2039method-of-use (U-4228)US 12343382
  • Jul 22, 2039method-of-use (U-4227)US 12343382
  • Jul 22, 2039method-of-use (U-4231)US 12343382
  • Jul 22, 2039method-of-use (U-4230)US 12343382
  • Jul 22, 2039method-of-use (U-4230)US 12343382
  • Jul 22, 2039method-of-use (U-4230)US 12343382
  • Jul 22, 2039method-of-use (U-4230)US 12343382
  • Jul 22, 2039method-of-use (U-4230)US 12343382
  • Jul 22, 2039method-of-use (U-4229)US 12343382
  • Jul 22, 2039method-of-use (U-4230)US 12343382
  • Jul 22, 2039method-of-use (U-4230)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4400)US 12343382
  • Jul 22, 2039method-of-use (U-4401)US 12343382
  • Jul 22, 2039method-of-use (U-4400)US 12343382
  • Jul 22, 2039method-of-use (U-4400)US 12343382
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4409)US 12343382
  • Jul 22, 2039method-of-use (U-4410)US 12343382
  • Jul 22, 2039method-of-use (U-4400)US 12343382
  • Jul 22, 2039method-of-use (U-4400)US 12343382
  • Jul 22, 2039method-of-use (U-4232)US 12343382
  • Jul 22, 2039method-of-use (U-4230)US 12343382
  • Jul 22, 2039method-of-use (U-4400)US 12343382
  • Jul 22, 2039method-of-use (U-4400)US 12343382
  • Jul 22, 2039method-of-use (U-4230)US 12343382
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4309)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4309)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4308)US 12453758
  • Jul 22, 2039method-of-use (U-4311)US 12453758
  • Jun 14, 2039compositionUS 11357820
  • Jun 14, 2039compositionUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039compositionUS 11357820
  • Jun 14, 2039compositionUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039compositionUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039compositionUS 11357820
  • Jun 14, 2039formulationUS 11357820
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-3855)US 11918623
  • Jun 14, 2039method-of-use (U-4377)US 12453755
  • Jun 14, 2039method-of-use (U-4385)US 12453755
  • Jun 14, 2039method-of-use (U-4386)US 12453755
  • Jun 14, 2039method-of-use (U-4378)US 12453755
  • Jun 14, 2039method-of-use (U-4386)US 12453755
  • Jun 14, 2039method-of-use (U-4381)US 12453755
  • Jun 14, 2039method-of-use (U-4380)US 12453755
  • Jun 14, 2039method-of-use (U-4377)US 12453755
  • Jun 14, 2039method-of-use (U-4378)US 12453755
  • Jun 14, 2039method-of-use (U-4386)US 12453755
  • Jun 14, 2039method-of-use (U-4376)US 12453755
  • Jun 14, 2039method-of-use (U-4383)US 12453755
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jun 14, 2039formulationUS 12453756
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
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  • Jan 5, 2036compositionUS 9474780
  • Jan 5, 2036compositionUS 9474780
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  • Jan 5, 2036compositionUS 9474780
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FDA exclusivities (62)

  • Dec 19, 2028NPPNew Product (3y)2.2y
  • Dec 19, 2028NPPNew Product (3y)2.2y
  • Dec 19, 2028NPPNew Product (3y)2.2y
  • Dec 19, 2028NPPNew Product (3y)2.2y
  • Dec 19, 2028NPPNew Product (3y)2.2y
  • Dec 19, 2028NPPNew Product (3y)2.2y
  • Dec 19, 2028NPPNew Product (3y)2.2y
  • Dec 19, 2028NPPNew Product (3y)2.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Dec 20, 2027I-958Indication (3y)1.2y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • Oct 18, 2027M-82Method (3y)1.0y
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • May 13, 2027NCENew Chemical Entity (5y)220d
  • Nov 8, 2026NPNP34d
  • Nov 8, 2026NPNP34d
  • Nov 8, 2026NPNP34d
  • Nov 8, 2026NPNP34d
  • Nov 8, 2026NPNP34d
  • Nov 8, 2026NPNP34d

News(10)

  • This week in charts: Kodiak’s big comeback and Hengrui’s dealmaking
    The latest installment in BioPharma Dive’s data visualization series features a closer look at Kodiak’s stock performance and Hengrui's ties with U.S. and European drugmakers.
    biopharma_dive · 2d ago
  • STAT+: Lilly bypasses Australian pharmacies with DTC model
    Eli Lilly is launching LillyDirect to deliver Mounjaro straight to Australian patients’ doors — and local doctors and pharmacists aren’t thrilled.
    stat · 2d ago
  • Kailera, Hengrui’s GLP-1/GIP candidate delivers weight, menstrual benefits to women with PMOS
    Kailera Therapeutics and Hengrui Pharma’s weekly injection showed benefits beyond weight loss in a mid-stage trial, leading to more regular menstrual cycles in patients with polyendocrine metabolic…
    biospace · 2d ago
  • 3 takeaways from a European obesity scientific meeting
    Eli Lilly impressed with its amylin-Zepbound combination data. Elsewhere, Novo demonstrated continued weight loss following a switch to oral and AbbVie and Boehringer gave glimpses into their conte…
    biopharma_dive · 3d ago
  • Fresenius Kabi manufacturing plant hit with FDA warning letter after adverse events
    Patients had adverse events after receiving a Fresenius Kabi medicine that experienced manufacturing deviations.
    biospace · 3d ago
  • STAT+: Pharmalittle: We’re reading about a plan to lower Medicare drug prices, a Lilly obesity drug, and more
    A final Medicare rule aimed at lowering prices for doctor-administered drugs applies to only four companies and saves 96% less than the initial proposal
    stat · 3d ago
  • Recon: Sanofi, Regeneron expand partnership after Dupixent success; Lilly amylin-Zepbound combo succeeds in mid-stage trial
    Welcome to Regulatory Reconnaissance, your regulatory news and intelligence briefing.
    raps · 4d ago
  • Superior weight loss, blood sugar control propel Lilly’s amylin-GIP/GLP-1 combo into Phase 3
    EloraTZP—a combination of an amylin asset and Eli Lilly’s approved obesity drug Zepbound—made a clean sweep of the primary and secondary endpoints in a mid-stage trial of adults with obesity and ty…
    biospace · 4d ago
  • #EASD26: Lilly's amylin-Zepbound combo posts best-ever weight loss in patients with obesity and diabetes
    MILAN — Forget Wegovy and Zepbound. Never mind CagriSema, and even retatrutide. The latest big name in obesity is eloraTZP. Data revealed Wednesday show that Lilly's amylin-incretin combination del…
    endpoints · 4d ago
  • STAT+: Eli Lilly’s Zepbound combined with amylin drug led to significant weight loss in mid-stage trial
    An investigational combination therapy from Eli Lilly led to significant weight loss in a mid-stage study, but high discontinuation rates raise questions about tolerability.
    stat · 4d ago
view all news mentions →
brand
ZEPBOUND
trade names
Mounjaro, Mounjaro (autoinjector), Zepbound, Zepbound (autoinjector)
generic
TIRZEPATIDE
MOA
12.1 Mechanism of Action Tirzepatide is a GIP receptor and GLP-1 receptor agonist. It contains a C20 fatty diacid that enables albumin binding and prolongs the half-life. Tirzepatide selectively binds to and activates both the GIP and GLP-1 receptors, the targets for native GIP and GLP-1. GLP-1 is a physiological regulator of appetite and caloric intake. Nonclinical studies suggest the addition of GIP may further contribute to the regulation of food intake. Both GIP receptors and GLP-1 receptors are found in areas of the brain involved in appetite regulation. Animal studies show that tirzepatide distributes to and activates neurons in brain regions involved in regulation of appetite and food intake.
indication
type 2 diabetes
phase
marketed
approved
2022-05-13
Data sources
openFDA · ClinicalTrials.gov · OpenTargets
last refreshed 3m ago
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