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  1. pharmadog
  2. ›drugs
  3. ›Humira
drug
save

adalimumab

Marketedupdated 5mo ago
by $ABBV AbbVie Inc.
Approved
annual revenue · 2024–2024peak $9.0B
2024: $9.0B2024$9.0B
community read0 votes

🐶 often sniffed alongside

top 8
  • tagApproval432 co-mentions · 155 sources
  • drugHUMIRA359 co-mentions · 156 sources
  • drugAMJEVITA168 co-mentions · 94 sources
  • drugABRILADA156 co-mentions · 88 sources
  • drugYUSIMRY152 co-mentions · 86 sources
  • company$ABBVAbbVie Inc.122 co-mentions · 61 sources
  • drugYUFLYMA28 co-mentions · 14 sources
  • drugHADLIMA26 co-mentions · 13 sources

Antibody drug with a maximum clinical stage of Approval (across all indications), with 14 approved and 20 investigational indications.

indications

investigational
IBD (Crohn's + UC)Rheumatoid Arthritis

all catalysts(61)

approval · 61
Dec 31, 2002
approval
$ABBV262.82+1.11%
24y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 12, 2003
approval
$ABBV262.82+1.11%
23y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jun 18, 2004
approval
$ABBV262.82+1.11%
22y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jul 30, 2004
approval
$ABBV262.82+1.11%
22y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Oct 3, 2005
approval
$ABBV262.82+1.11%
21y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Oct 3, 2005
approval
$ABBV262.82+1.11%
21y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jun 23, 2006
approval
$ABBV262.82+1.11%
20y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jul 28, 2006
approval
$ABBV262.82+1.11%
20y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Nov 9, 2006
approval
$ABBV262.82+1.11%
20y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Nov 9, 2006
approval
$ABBV262.82+1.11%
20y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Feb 16, 2007
approval
$ABBV262.82+1.11%
20y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Feb 27, 2007
approval
$ABBV262.82+1.11%
20y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jul 30, 2007
approval
$ABBV262.82+1.11%
19y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 5, 2007
approval
$ABBV262.82+1.11%
19y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jan 18, 2008
approval
$ABBV262.82+1.11%
19y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Feb 21, 2008
approval
$ABBV262.82+1.11%
19y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Mar 11, 2009
approval
$ABBV262.82+1.11%
18y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Apr 8, 2010
approval
$ABBV262.82+1.11%
17y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jul 29, 2010
approval
$ABBV262.82+1.11%
16y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 29, 2010
approval
$ABBV262.82+1.11%
16y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Nov 18, 2010
approval
$ABBV262.82+1.11%
16y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Feb 25, 2011
approval
$ABBV262.82+1.11%
16y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Mar 14, 2011
approval
$ABBV262.82+1.11%
16y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jul 13, 2011
approval
$ABBV262.82+1.11%
15y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 7, 2011
approval
$ABBV262.82+1.11%
15y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Dec 13, 2011
approval
$ABBV262.82+1.11%
15y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Dec 26, 2011
approval
$ABBV262.82+1.11%
15y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
May 24, 2012
approval
$ABBV262.82+1.11%
14y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 28, 2012
approval
$ABBV262.82+1.11%
14y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Apr 24, 2013
approval
$ABBV262.82+1.11%
13y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
May 13, 2013
approval
$ABBV262.82+1.11%
13y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 19, 2013
approval
$ABBV262.82+1.11%
13y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Feb 26, 2014
approval
$ABBV262.82+1.11%
13y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
May 14, 2014
approval
$ABBV262.82+1.11%
12y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
May 30, 2014
approval
$ABBV262.82+1.11%
12y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Aug 7, 2014
approval
$ABBV262.82+1.11%
12y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 23, 2014
approval
$ABBV262.82+1.11%
12y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 30, 2014
approval
$ABBV262.82+1.11%
12y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Oct 29, 2014
approval
$ABBV262.82+1.11%
12y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Nov 6, 2014
approval
$ABBV262.82+1.11%
12y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Dec 24, 2014
approval
$ABBV262.82+1.11%
12y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 9, 2015
approval
$ABBV262.82+1.11%
11y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Nov 23, 2015
approval
$ABBV262.82+1.11%
11y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jun 30, 2016
approval
$ABBV262.82+1.11%
10y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Oct 17, 2016
approval
$ABBV262.82+1.11%
10y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Mar 27, 2017
approval
$ABBV262.82+1.11%
10y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Apr 21, 2017
approval
$ABBV262.82+1.11%
9y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Apr 28, 2017
approval
$ABBV262.82+1.11%
9y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Dec 14, 2017
approval
$ABBV262.82+1.11%
9y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Aug 2, 2018
approval
$ABBV262.82+1.11%
8y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Sep 28, 2018
approval
$ABBV262.82+1.11%
8y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Oct 16, 2018
approval
$ABBV262.82+1.11%
8y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Dec 6, 2018
approval
$ABBV262.82+1.11%
8y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jan 11, 2019
approval
$ABBV262.82+1.11%
8y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Mar 11, 2020
approval
$ABBV262.82+1.11%
7y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Dec 16, 2020
approval
$ABBV262.82+1.11%
6y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Dec 16, 2020
approval
$ABBV262.82+1.11%
6y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Feb 24, 2021
approval
$ABBV262.82+1.11%
6y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Nov 3, 2023
approval
$ABBV262.82+1.11%
3y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Jul 16, 2025
approval
$ABBV262.82+1.11%
1y ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
Dec 23, 2025
approval
$ABBV262.82+1.11%
10mo ago
HUMIRA (ADALIMUMAB) — FDA approval
adalimumab
→
view all 61 catalysts →

Trials studying adalimumab

  • phase4A Clinical Trial of Taibowei® Adalimumab Injection in the Treatment of Chinese Pediatric Patients With Moderately to Severely Active Crohn's Diseaserecruitingn=30
  • phase3A Study to Assess Adverse Events, Change in Disease Activity, and How the Drug Moves Through the Body in Children With Juvenile Psoriatic Arthritis (jPsA) Receiving Subcutaneously Injected Risankizumab or Adalimumabrecruitingn=40
  • phase3Study to Assess Change in Disease Activity and Adverse Events of Oral Upadacitinib Compared to Subcutaneous Adalimumab in Adult Participants With Moderate to Severe Rheumatoid Arthritiscompletedn=487
  • phase1A Study of Pharmacokinetics, Safety, and Immunogenicity of BCD-057 100 mg/mL, BCD-057 50 mg/mL, and Humira 100 mg/mL in Healthy Subjectscompletedn=444
  • phase4A Multicenter, Open-label Study on the Efficacy and Safety of Tebiovio® (Adalimumab) in Treating Chinese Children With Severe Plaque Psoriasisrecruitingn=30
  • phase4A Study of Vedolizumab Intravenous (IV) and Adalimumab or Vedolizumab and Ustekinumab in Adults With Crohn's Diseaserecruitingn=100
  • phase3A Study of Baricitinib (LY3009104) in Participants From 2 Years to Less Than 18 Years Old With Active JIA-Associated Uveitis or Chronic Anterior Antinuclear Antibody-Positive Uveitisactive not recruitingn=30
  • phase3A Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque Psoriasiscompletedn=478

News(9)

  • BMO most bullish on Merck's, bearish on BMS’ plans to contend with patent cliffs
    BMO Capital Markets is more impressed by Merck’s plans to replace lost Keytruda revenue than on Bristol Myers Squibb’s efforts to fill the expected void that will come from loss of exclusivity for…
    biospace · 3d ago
  • Merck’s antibody impresses with ‘highly competitive’ data in chronic skin disease
    Merck has revealed detailed data for tulisokibart from a mid-stage trial in hidradenitis suppurativa that analysts say could help carve out a place in a crowded market that already includes AbbVie’…
    biospace · 4d ago
  • 6 immunology targets to sustain a mammoth I&I market
    Johnson & Johnson, Pfizer, Argenx and more are unlocking new immunology targets and looking to improve on existing ones in an attempt to catch some of the magic brought about by AbbVie’s Humira and…
    biospace · 7d ago
  • Drugmakers cherry pick launch regions as MFN creates 'policy environment like an earthquake'
    With multiple drug pricing initiatives like Most Favored Nation now in force, drugmakers have to reinvent their commercial strategies to stay ahead of the fast-moving policy environment, according…
    biospace · 25d ago
  • MoonLake’s nanobody boosts all clinical endpoints in phase 3 psoriatic arthritis trial
    MoonLake Immunotherapeutics announced positive phase 3 data for patients with psoriatic arthritis treated with its lead nanobody candidate, sonelokimab.
    fiercebiotech · 1mo ago
  • AbbVie shares pressured as Q2 I&I beat falls below investor expectations
    AbbVie investors’ sky-high expectations led to a 4% share decline on Friday as the company reported more modest consensus beats than expected.
    biospace · 2mo ago
  • cAMPfield lands $180M to build gut disease drug
    The biotech is advancing an anti-inflammatory drug that originated with vTv for inflammatory bowel diseases, leaning on a better side effect profile.
    biopharma_dive · 3mo ago
  • Biogen adds more immune drugs in $1B buyout of secretive startup RayThera
    The companies didn’t specify the drugs Biogen is acquiring in the deal, though patents RayThera secured provide important clues.
    biopharma_dive · 3mo ago
  • Opinion: The podcast telling the stories behind Ambien, Ozempic, EpiPens, and other game-changing drugs
    “We're basically not using our body as directed,” says "Drug Story" host Thomas Goetz.
    stat · 5mo ago
brand
Humira
generic
adalimumab
MOA
12.1 Mechanism of Action Adalimumab binds specifically to TNF-alpha and blocks its interaction with the p55 and p75 cell surface TNF receptors. Adalimumab also lyses surface TNF expressing cells in vitro in the presence of complement. Adalimumab does not bind or inactivate lymphotoxin (TNF-beta). TNF is a naturally occurring cytokine that is involved in normal inflammatory and immune responses. Elevated concentrations of TNF are found in the synovial fluid of patients with RA, JIA, PsA, and AS and play an important role in both the pathologic inflammation and the joint destruction that are hallmarks of these diseases. Increased concentrations of TNF are also found in psoriasis plaques. In Ps, treatment with HUMIRA may reduce the epidermal thickness and infiltration of inflammatory cells. The relationship between these pharmacodynamic activities and the mechanism(s) by which HUMIRA exerts its clinical effects is unknown. Adalimumab also modulates biological responses that are induced or regulated by TNF, including changes in the concentrations of adhesion molecules responsible for leukocyte migration (ELAM-1, VCAM-1, and ICAM-1 with an IC 50 of 1-2 X 10 -10 M).
indication
Intermediate Uveitis
phase
marketed
approved
2002-12-31
Data sources
openFDA · ClinicalTrials.gov
last refreshed 38m ago
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