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  1. pharmadog
  2. ›drugs
  3. ›Keytruda
drug · antibody
save

pembrolizumab

Marketedupdated 4mo ago
by $MRK Merck & Co., Inc.🔗 ChEMBL
Approved
annual revenue · 2024–2024peak $29.5B
2024: $29.5B2024$29.5B
community read0 votes

🐶 often sniffed alongside

top 8
  • drugKEYTRUDA515 co-mentions · 131 sources
  • tagApproval512 co-mentions · 128 sources
  • drugKEYTRUDA QLEX269 co-mentions · 131 sources
  • drugCancer Program256 co-mentions · 128 sources
  • drug(berahyaluronidase alfa + pembrolizumab)10 co-mentions · 5 sources
  • tagGlioblastoma2 co-mentions · 1 sources
  • drugaxelopran1 co-mentions · 1 sources
  • companyNational Institute of Neurological Disorders and Stroke1 co-mentions · 1 sources

Antibody drug with a maximum clinical stage of Approval (across all indications), with 9 approved and 146 investigational indications.

indications

investigational
NSCLCMelanoma

targets

Programmed cell death protein 1

all catalysts(100)

approval · 100
Sep 4, 2014
approval
12y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 19, 2015
approval
11y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 2, 2015
approval
11y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Dec 18, 2015
approval
11y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Dec 18, 2015
approval
11y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 5, 2016
approval
10y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 24, 2016
approval
10y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 24, 2016
approval
10y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Mar 14, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
May 10, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
May 17, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
May 18, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
May 18, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
May 23, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jul 27, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jul 27, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Sep 22, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Nov 29, 2017
approval
9y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 12, 2018
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 13, 2018
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 19, 2018
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 16, 2018
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 20, 2018
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 30, 2018
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Nov 9, 2018
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Dec 19, 2018
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Dec 28, 2018
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Feb 15, 2019
approval
8y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 11, 2019
approval
7y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 19, 2019
approval
7y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 10, 2019
approval
7y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 17, 2019
approval
7y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jul 30, 2019
approval
7y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jul 30, 2019
approval
7y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Sep 17, 2019
approval
7y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jan 8, 2020
approval
7y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jan 9, 2020
approval
7y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 28, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 16, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 16, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 24, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 24, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 29, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 2, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 14, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Nov 10, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Nov 13, 2020
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Feb 10, 2021
approval
6y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Mar 16, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Mar 16, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Mar 22, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Mar 30, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
May 5, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 28, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jul 1, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jul 21, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jul 26, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jul 26, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 3, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 10, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 31, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 31, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 13, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 13, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Nov 17, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Dec 3, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Dec 17, 2021
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Feb 4, 2022
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Feb 4, 2022
approval
5y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Mar 21, 2022
approval
4y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
May 20, 2022
approval
4y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jun 21, 2022
approval
4y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 5, 2022
approval
4y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Dec 16, 2022
approval
4y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Jan 26, 2023
approval
4y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Mar 28, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Apr 3, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 14, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Aug 14, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 12, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 16, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 23, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 31, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Oct 31, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Nov 7, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
Nov 16, 2023
approval
3y ago
KEYTRUDA (PEMBROLIZUMAB) — FDA approval
pembrolizumab
→
view all 100 catalysts →

Trials studying pembrolizumab

  • phase3Safety, Efficacy, and Pharmacokinetics of BNT327 in Combination With Chemotherapy and Other Investigational Agents for Lung Cancerrecruitingn=1,580
  • phase2Study to Evaluate Adverse Events and Efficacy of Intravenous (IV) Telisotuzumab Adizutecan in Combination With a PD-1 Immune Checkpoint Inhibitor in Adult Participants With Advanced or Metastatic Non-Squamous NSCLC With No Prior Treatment for Advanced Disease, and No Actionable Genomic Alterationsrecruitingn=252
  • phase3A Study of Sacituzumab Tirumotecan (MK-2870) as a Single Agent and in Combination With Pembrolizumab (MK-3475) Versus Treatment of Physician's Choice in Participants With HR+/HER2- Unresectable Locally Advanced or Metastatic Breast Cancer (MK-2870-010)recruitingn=1,200
  • phase3A Clinical Trial of Three Study Medicines (Encorafenib, Binimetinib, and Pembrolizumab) in Patients With Advanced or Metastatic Melanomaactive not recruitingn=257
  • phase3Beamion LUNG-3: Adjuvant Zongertinib vs Standard Treatment in People With Completely Resected Stage II-IIIB NSCLC Harboring Activating HER2 TKD Mutationsrecruitingn=400
  • phase1A Clinical Study of MK-4716 in People With Certain Solid Tumors (MK-4716-001)recruitingn=250
  • phase3Safety and Efficacy of Lenvatinib (E7080/MK-7902) With Pembrolizumab (MK-3475) in Combination With Transarterial Chemoembolization (TACE) in Participants With Incurable/Non-metastatic Hepatocellular Carcinoma (MK-7902-012/E7080-G000-318/LEAP-012)terminatedn=480
  • phase2A Study of SKB571 Combination Therapy in Participants With Non-Small Cell Lung Cancer (NSCLC)recruitingn=150
more trials →

News(10)

  • Merck's top dealmaker signals more M&A as Keytruda's patent cliff nears
    Merck CEO Robert Davis has been landing deals “with urgency” over the last few years in an effort to shore up the pipeline ahead of Keytruda’s upcoming patent cliff. But make no mistake: The compan…
    endpoints · 1d ago
  • Summit, Akeso’s ivonescimab bests Merck’s Keytruda in China trial—again
    New Phase 3 data show that Summit Therapeutics and Akeso’s PD-1/VEGF therapy improved overall survival in patients with a type of lung cancer as compared to Merck’s Keytruda but the results will ne…
    biospace · 1d ago
  • Akeso, Summit cancer drug confirms lung cancer survival benefit
    A new data cut of a trial pitting ivonescimab, a bispecific antibody, against Merck’s Keytruda showed the new drug helped people live longer.
    biopharma_dive · 1d ago
  • Novartis inks $3.2B subcutaneous drug delivery deal with Alteogen
    Novartis has struck a deal worth up to $3.2 billion to work with Alteogen on subcutaneous drug delivery, joining Biogen and GSK on the list of drugmakers to pay to access the technology this year.
    fiercebiotech · 3d ago
  • Stripped of AstraZeneca safety net, BMS could face ‘carnage’ if high-risk clinical trial fails
    BMS is barreling toward a clinical trial readout that an H.C. Wainwright analyst believes could contribute to the return of mergers between mega-cap drugmakers.
    biospace · 3d ago
  • BioNTech halts mid-stage trial of personalized mRNA vaccine in colorectal cancer
    Shares of Germany-based BioNTech were down as much as 8% Friday after announcing a Phase 2 trial of autogene cevumeran would be discontinued for futility. The news follows Merck and Moderna’s Phase…
    biospace · 7d ago
  • BioNTech-Genentech cancer vax records more deaths than control in scrapped ph. 2 test
    Following Merck and Moderna’s phase 3 triumph with a Keytruda-paired personalized mRNA cancer vaccine, a similar shot from BioNTech and Genentech has faltered in a reminder of the approach’s strugg…
    fiercebiotech · 7d ago
  • Revolution pancreatic cancer drug should quickly become a blockbuster, analysts say
    Rasonque’s $39,800 monthly list price surpassed Wall Street forecasts and led to rosier sales projections ahead of what one analyst described as a “historic” launch.
    biopharma_dive · 8d ago
  • What’s in Merck and Moderna’s cancer vaccine algorithm?
    A heart drug failure, RevMed's pancreatic cancer drug approved, and more biotech news from The Readout
    stat · 8d ago
  • Summit, Akeso tout biliary cancer win for PD-1/VEGF in China—but details are pending
    The Phase 3 readout is the first for ivonescimab beyond non-small cell lung cancer to show a significant overall survival benefit, according to Summit Therapeutics and China-based partner Akeso.
    biospace · 9d ago
view all news mentions →
brand
Keytruda
trade names
Keytruda, Pembrolizumab component of mk 7684a, Pembrolizumab component of mk-1308a
generic
pembrolizumab
MOA
Programmed cell death protein 1 inhibitor
indication
Merkel Cell Carcinoma
phase
marketed
approved
2014-09-04
Data sources
openFDA · ClinicalTrials.gov · OpenTargets
last refreshed 2h ago
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