Briakinumab

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Briakinumab
Monoclonal antibody
Type Whole antibody
Source Human
Target IL-12 and IL-23
Legal status
Legal status
  • investigational
Pharmacokinetic data
Bioavailability N/A
Identifiers
CAS Number 339308-60-0 N
ATC code L04AC09 (WHO)
ChemSpider none
UNII 978I8M0P8X YesY
Chemical data
Formula C6376H9874N1722O1992S44
Molar mass 146.5 kg/mol
 NYesY (what is this?)  (verify)

Briakinumab (ABT-874) is a human monoclonal antibody being developed by Abbott Laboratories for the treatment of rheumatoid arthritis, inflammatory bowel disease, and multiple sclerosis. As of 2011 drug development for psoriasis has been discontinued in the U.S. and Europe.[1]

Like ustekinumab, the antibody targets the interleukins 12 and 23.[2]

Discovery[edit]

The candidate drug was discovered by Cambridge Antibody Technology in collaboration with Abbott.[3][4]

Trials[edit]

As of November 2009, Phase III clinical trials for plaque psoriasis[5][6] and a Phase II trial for multiple sclerosis[7] have been completed, and a Phase II trial for Crohn's disease is underway.[8]

Briakinumab was compared to etanercept and placebo in several double-blind trials. The Psoriasis Area Severity Index (PASI) was reduced significantly better than under the comparator treatments. 81–82% of patients under briakinumab, 40–56% under etanercept, and 7% under placebo reached PASI reduction of at least 75%.[9] No head-to-head studies against ustekinumab, the other IL-12/23 inhibitor, are available.

On January 15, 2011, Abbott announced the withdrawal of its application to the US FDA and European regulators for briakinumab. Following feedback from regulatory authorities indicating the need for further analysis, including the potential for additional studies, Abbott withdrew its applications and was evaluating next steps including possible resubmission at a later date. This compound has never been resubmitted for approval.

Royalties[edit]

This is the second candidate from a deal with Cambridge Antibody Technology that Abbott have taken to late-stage clinical trials. As a result of the protracted royalty dispute over Humira Abbott agreed to pay CAT a reduced royalty of 4.75% on any future sales of ABT-874, from which CAT will pay a portion to the MRC and other licensors (according to CAT's 1997 agreement with the MRC).[10]

References[edit]

  1. ^ "Abbott withdraws briakinumab applications in USA, Europe". PharmaTimes. 17 January 2011. 
  2. ^ Lima, X. T.; Abuabara, K.; Kimball, A. B.; Lima, H. C. (2009). "Briakinumab". Expert Opinion on Biological Therapy. 9 (8): 1107–13. doi:10.1517/14712590903092188. PMID 19569977. 
  3. ^ "Abbott 2007 Annual Report: Pharmaceuticals". Abbott.com. Retrieved 2010-05-12. 
  4. ^ MedImmune: External R&D Partnering
  5. ^ Clinical trial number NCT00570986 for "A Study Comparing the Safety and Efficacy of Two Dosing Regimens of ABT-874 to Placebo in Subjects With Moderate to Severe Chronic Plaque Psoriasis" at ClinicalTrials.gov
  6. ^ Clinical trial number NCT00691964 for "Study Comparing the Efficacy and Safety of ABT-874 to Etanercept and Placebo in Subjects With Moderate to Severe Chronic Plaque Psoriasis" at ClinicalTrials.gov
  7. ^ Clinical trial number NCT00086671 for "Safety and Effectiveness of Two Doses of ABT-874 as Compared to Placebo in Subjects With Multiple Sclerosis (MS)" at ClinicalTrials.gov
  8. ^ Clinical trial number NCT00562887 for "Dose Ranging Study Comparing the Efficacy, Safety and Pharmacokinetics of Intravenous Infusions of ABT-874 vs Placebo in Subjects With Active Crohn's Disease" at ClinicalTrials.gov
  9. ^ Abbott Press Release: Abbott Reports Psoriasis Phase III Results of its Investigational IL-12/23 Inhibitor Briakinumab (ABT-874)
  10. ^ The Free Library: Cambridge Antibody Technology and Abbott Agree Regarding Royalties