Brensocatib

Highest phase reached
Drug type
Small molecule

Listing at source
Listed
Highest phase reached

Drug type
Small molecule
Drug name
Brensocatib
Molecular weight
Structure (SMILES)
Cn1c(=O)oc2ccc(-c3ccc(C[C@@H](C#N)NC(=O)[C@@H]4CNCCCO4)cc3)cc21

  • azd 7986
  • AZD 7986
  • Azd-7986
  • AZD-7986
  • azd7986
  • Azd7986
  • AZD7986
  • brensocatib
  • Brensocatib
  • brensocatib [INN]
  • BRENSOCATIB [USAN]
  • Brensocatib [WHO-DD]
  • Brensocatib 10 mg
  • Brensocatib 25 mg
  • brensocatib inn
  • Brensocatib Oral Solution
  • Brensocatib Oral Tablet
  • brensocatib usan
  • brensocatib who dd
  • ins 1007
  • INS-1007
  • ins1007
  • INS1007

ATC classification codes
  • R03
CAS registry numbers
  • 1802148-05-5
ChEMBL ID
CHEMBL3900409
InChIKey
AEXFXNFMSAAELR-RXVVDRJESA-N
PubChem compound IDs
  • 118253852
RxNorm IDs (RxCUI)
  • 2721880
FDA ingredient codes (UNII)
  • 25CG88L0BB

Status
Authorised
Status date
18 Nov 2025
Authorisation date
18 Nov 2025
Approved indications
Brinsupri is indicated for the treatment of non-cystic fibrosis bronchiectasis (NCFB) in patients 12 years of age and older with two or more exacerbations in the prior 12 months.
Product number
EMEA/H/C/005820
Authorisation holder
Insmed Netherlands B.V.
Priority medicines scheme
Yes
Generic
No
Biosimilar
No
Generic medicines
0
Biosimilar medicines
0
Advanced therapy
No
Conditional approval
No
Additional monitoring
Yes
Accelerated assessment
No
Exceptional circumstances
No

Therapeutic areas

  • Bronchiectasis
  • Lung Diseases
European medicines record

Patents
14
Designations
5
Earliest recorded loss of exclusivity
21 Feb 2040
First in class
No
Fast track
No
Breakthrough designation
Yes
Orphan designation
No
Priority review
Yes
Orphan exclusivity
No
Accelerated approval
No

Pharmacology name
brensocatib
Type
Synthetic organic
Drug name stem
-catib
Approval recorded by Guide to Pharmacology
Yes

  • Action
    Inhibition
    Action type
    Inhibitor
    Target
    cathepsin C
    Gene symbol
    CTSC
    Protein identifier
    P53634
    Median affinity
    8.4
    Affinity units
    pIC50
    Primary target
    Yes
  • Mechanism
    Dipeptidyl peptidase I inhibitor
    Action type
    Inhibitor
    Target
    Dipeptidyl peptidase 1
    Protein identifier
    P53634

Open Targets mechanisms

  • Mechanism
    Dipeptidyl peptidase I inhibitor
    Action type
    Inhibitor
    Target
    Dipeptidyl peptidase 1

  • Condition
    Liver Diseases
    Highest recorded phase
    1
    Condition identifier
    EFO:0001421
    Subject identifier
    D008107
  • Condition
    Kidney Diseases
    Highest recorded phase
    1
    Condition identifier
    EFO:0003086
    Subject identifier
    D007674
  • Condition
    Bronchiectasis
    Highest recorded phase
    3
    Condition identifier
    HP:0002110
    Subject identifier
    D001987
  • Condition
    Bronchiectasis
    Highest recorded phase
    3
    Condition identifier
    MONDO:0004822
    Subject identifier
    D001987
  • Condition
    Cystic Fibrosis
    Highest recorded phase
    2
    Condition identifier
    MONDO:0009061
    Subject identifier
    D003550
  • Condition
    Severe Acute Respiratory Syndrome
    Highest recorded phase
    3
    Condition identifier
    MONDO:0100096
    Subject identifier
    D045169

  • Condition identifier
    EFO_0001421
    Highest recorded phase
    1
  • Condition identifier
    EFO_0003086
    Highest recorded phase
    1
  • Condition identifier
    EFO_0003818
  • Condition identifier
    EFO_1000710
    Highest recorded phase
    2
  • Condition identifier
    EFO_1002030
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0004822
  • Condition identifier
    MONDO_0004822
    Highest recorded phase
    4
  • Condition identifier
    MONDO_0005275
    Highest recorded phase
    4
  • Condition identifier
    MONDO_0006502
    Highest recorded phase
    3
  • Condition identifier
    MONDO_0006559
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0009061
    Highest recorded phase
    2
  • Condition identifier
    MONDO_0100096
    Highest recorded phase
    3

Hydrogen bond acceptors
7
Hydrogen bond donors
2
Polar surface area
109.29
Calculated partition coefficient (ALogP)
1.73
Calculated partition coefficient (XLogP)
2
Prodrug
No
Chirality
Single enantiomer
Inorganic
No
Rule-of-five violations
0
Rotatable bonds
5
Heavy atoms
31
Molecular formula
C23H24N4O4
Monoisotopic mass
420.17975526
Natural product
No

  • 71558-001
  • 71558-002

Recorded assays
108
Active assays
37

  • Confirmatory
  • Other

These details could not be displayed.

Related records

Trials (18)

In development for (6)

Other linked conditions (1)

Targets (1)