Bevacizumab

Highest phase reached
Drug type
First approval year

First approval year
Listing at source
Listed
Highest phase reached

Drug type
Drug name
Bevacizumab

  • abevmy
  • Abevmy
  • alymsys
  • Alymsys
  • avastin
  • Avastin
  • avzivi
  • Avzivi
  • aybintio
  • Aybintio
  • equidacent
  • Equidacent
  • lextemy
  • Lextemy
  • mvasi
  • Mvasi
  • onbevzi
  • Onbevzi
  • oyavas
  • Oyavas
  • vegzelma
  • Vegzelma
  • zirabev
  • Zirabev

  • 1 25mg bevacizumab
  • 1.25mg bevacizumab
  • 12 igg1
  • 12-IGG1
  • 2.50mg bevacizumab
  • abp 215
  • ABP 215
  • Abp-215
  • alymsys
  • Alymsys
  • ava 1
  • AVA-1
  • avastin
  • Avastin
  • AVASTIN
  • Avastin (bevacizumab)
  • Avastin (Bevacizumab)
  • Avastin(Bevacizumab)
  • Avastin®
  • Avastin® (bevacizumab)
  • avzivi
  • Avzivi
  • bat 1706
  • Bat 1706
  • BAT 1706 [WHO-DD]

And 256 more, listed on the interactive page.

CAS registry numbers
  • 216974-75-3
ChEMBL ID
CHEMBL1201583
FDA ingredient codes (UNII)
  • 2S9ZZM9Q9V

  • L01FG01
  • L01XC07
  • S01LA04
  • S01LA08
Sources for recorded values

  • 253337
  • 2599041

Applicant
GENENTECH
Approval date
26 Feb 2004
Application number
BLA125085

Status
Authorised
Status date
12 Jan 2005
Authorisation date
12 Jan 2005
Approved indications
Bevacizumab in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. Bevacizumab in combination with paclitaxel is indicated for first-line treatment of adult patients with metastatic breast cancer. For further information as to human epidermal growth factor receptor 2 (HER2) status. Bevacizumab in combination with capecitabine is indicated for first-line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. Patients who have received taxane and anthracycline-containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with Avastin in combination with capecitabine. For further information as to HER2 status. Bevacizumab, in addition to platinum-based chemotherapy, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer other than predominantly squamous cell histology. Bevacizumab, in combination with erlotinib, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-squamous non-small cell lung cancer with Epidermal Growth Factor Receptor (EGFR) activating mutations. Bevacizumab in combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. Bevacizumab, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of adult patients with advanced (International Federation of Gynecology and Obstetrics (FIGO) stages III B, III C and IV) epithelial ovarian, fallopian tube, or primary peritoneal cancer.Bevacizumab, in combination with carboplatin and gemcitabine, is indicated for treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor–targeted agents. Bevacizumab in combination with paclitaxel, topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum-resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor–targeted agents. Bevacizumab, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix.
Product number
EMEA/H/C/000582
Authorisation holder
Roche Registration GmbH
Priority medicines scheme
No
Generic
No
Biosimilar
No
Generic medicines
0
Biosimilar medicines
8
Advanced therapy
No
Conditional approval
No
Additional monitoring
No
Accelerated assessment
No
Exceptional circumstances
No

Therapeutic areas

  • Breast Neoplasms
  • Carcinoma, Non-Small-Cell Lung
  • Carcinoma, Renal Cell
  • Colorectal Neoplasms
  • Fallopian Tube Neoplasms
  • Ovarian Neoplasms
  • Peritoneal Neoplasms
  • Uterine Cervical Neoplasms
European medicines record

Patents
0
Designations
5
Earliest recorded loss of exclusivity
29 May 2027
First in class
No
Fast track
Yes
Breakthrough designation
Yes
Orphan designation
No
Priority review
Yes
Orphan exclusivity
No
Accelerated approval
No
Availability
Prescription only

Pharmacology name
bevacizumab
Type
Antibody
Drug name stem
-mab; -mab
Approval recorded by Guide to Pharmacology
Yes

Administration routes

  • Parenteral

  • Action
    Binding
    Action type
    Binding
    Target
    VEGFA
    Gene symbol
    VEGFA
    Affinity units
    pIC50
    Primary target
    Yes
  • Mechanism
    Vascular endothelial growth factor A inhibitor
    Action type
    Inhibitor
    Target
    Vascular endothelial growth factor A, long form
    Protein identifier
    P15692

Open Targets mechanisms

  • Mechanism
    Vascular endothelial growth factor A inhibitor
    Action type
    Inhibitor
    Target
    Vascular endothelial growth factor A, long form

  • Condition
    Leukemia, Lymphocytic, Chronic, B-Cell
    Highest recorded phase
    2
    Condition identifier
    EFO:0000095
    Subject identifier
    D015451
  • Condition
    Lymphoma, Follicular
    Highest recorded phase
    3
    Condition identifier
    EFO:0000096
    Subject identifier
    D008224
  • Condition
    Stomach Neoplasms
    Highest recorded phase
    3
    Condition identifier
    EFO:0000178
    Subject identifier
    D013274
  • Condition
    Carcinoma, Squamous Cell
    Highest recorded phase
    2
    Condition identifier
    EFO:0000181
    Subject identifier
    D002294
  • Condition
    Carcinoma, Hepatocellular
    Highest recorded phase
    3
    Condition identifier
    EFO:0000182
    Subject identifier
    D006528
  • Condition
    Hodgkin Disease
    Highest recorded phase
    2
    Condition identifier
    EFO:0000183
    Subject identifier
    D006689
  • Condition
    Prostatic Neoplasms
    Highest recorded phase
    3
    Condition identifier
    EFO:0000196
    Subject identifier
    D011471
  • Condition
    Myelodysplastic Syndromes
    Highest recorded phase
    2
    Condition identifier
    EFO:0000198
    Subject identifier
    D009190
  • Condition
    Neoplasms, Plasma Cell
    Highest recorded phase
    2
    Condition identifier
    EFO:0000200
    Subject identifier
    D054219
  • Condition
    Adenocarcinoma
    Highest recorded phase
    3
    Condition identifier
    EFO:0000228
    Subject identifier
    D000230
  • Condition
    Adenoma
    Highest recorded phase
    2
    Condition identifier
    EFO:0000232
    Subject identifier
    D000236
  • Condition
    Rhabdomyosarcoma, Alveolar
    Highest recorded phase
    2
    Condition identifier
    EFO:0000248
    Subject identifier
    D018232
  • Condition
    Astrocytoma
    Highest recorded phase
    2
    Condition identifier
    EFO:0000272
    Subject identifier
    D001254
  • Condition
    Breast Neoplasms
    Highest recorded phase
    4
    Condition identifier
    EFO:0000305
    Subject identifier
    D001943
  • Condition
    Carcinoma
    Highest recorded phase
    2
    Condition identifier
    EFO:0000313
    Subject identifier
    D002277
  • Condition
    Glioma
    Highest recorded phase
    2
    Condition identifier
    EFO:0000326
    Subject identifier
    D005910
  • Condition
    Carcinoma, Renal Cell
    Highest recorded phase
    4
    Condition identifier
    EFO:0000335
    Subject identifier
    D002292
  • Condition
    Leukemia, Myelogenous, Chronic, BCR-ABL Positive
    Highest recorded phase
    2
    Condition identifier
    EFO:0000339
    Subject identifier
    D015464
  • Condition
    Adenocarcinoma, Clear Cell
    Highest recorded phase
    2
    Condition identifier
    EFO:0000348
    Subject identifier
    D018262
  • Condition
    Carcinoma, Renal Cell
    Highest recorded phase
    4
    Condition identifier
    EFO:0000349
    Subject identifier
    D002292
  • Condition
    Colorectal Neoplasms
    Highest recorded phase
    4
    Condition identifier
    EFO:0000365
    Subject identifier
    D015179
  • Condition
    Melanoma
    Highest recorded phase
    2
    Condition identifier
    EFO:0000389
    Subject identifier
    D008545
  • Condition
    Lymphoma, Large B-Cell, Diffuse
    Highest recorded phase
    2
    Condition identifier
    EFO:0000403
    Subject identifier
    D016403
  • Condition
    Carcinoma, Endometrioid
    Highest recorded phase
    2
    Condition identifier
    EFO:0000466
    Subject identifier
    D018269
  • Condition
    Stomach Neoplasms
    Highest recorded phase
    3
    Condition identifier
    EFO:0000503
    Subject identifier
    D013274

And 193 more, listed on the interactive page.

  • Condition identifier
    EFO_0000095
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000096
    Highest recorded phase
    3
  • Condition identifier
    EFO_0000181
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000182
    Highest recorded phase
    3
  • Condition identifier
    EFO_0000183
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000198
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000200
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000272
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000280
  • Condition identifier
    EFO_0000313
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000348
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000349
  • Condition identifier
    EFO_0000365
  • Condition identifier
    EFO_0000389
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000503
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000514
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000519
  • Condition identifier
    EFO_0000558
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000571
    Highest recorded phase
    3
  • Condition identifier
    EFO_0000574
    Highest recorded phase
    3
  • Condition identifier
    EFO_0000588
  • Condition identifier
    EFO_0000616
  • Condition identifier
    EFO_0000621
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000632
    Highest recorded phase
    2
  • Condition identifier
    EFO_0000637
    Highest recorded phase
    2

And 386 more, listed on the interactive page.

  • Event
    anaemia
    Reports
    2,208
    Reporting signal score
    904.913
  • Event
    bone marrow failure
    Reports
    821
    Reporting signal score
    970.871
  • Event
    diarrhoea
    Reports
    3,647
    Reporting signal score
    740.175
  • Event
    disease progression
    Reports
    2,511
    Reporting signal score
    2,910.6
  • Event
    endophthalmitis
    Reports
    690
    Reporting signal score
    1,576.28
  • Event
    epistaxis
    Reports
    1,106
    Reporting signal score
    866.558
  • Event
    febrile neutropenia
    Reports
    1,106
    Reporting signal score
    737.25
  • Event
    gastrointestinal perforation
    Reports
    561
    Reporting signal score
    1,480.64
  • Event
    hypertension
    Reports
    3,475
    Reporting signal score
    3,057.49
  • Event
    intestinal perforation
    Reports
    421
    Reporting signal score
    692.593
  • Event
    mucosal inflammation
    Reports
    760
    Reporting signal score
    764.949
  • Event
    myelosuppression
    Reports
    642
    Reporting signal score
    1,077.88
  • Event
    neuropathy peripheral
    Reports
    1,346
    Reporting signal score
    846.499
  • Event
    neutropenia
    Reports
    1,974
    Reporting signal score
    1,045.46
  • Event
    neutrophil count decreased
    Reports
    913
    Reporting signal score
    834.103
  • Event
    palmar-plantar erythrodysaesthesia syndrome
    Reports
    925
    Reporting signal score
    1,242.05
  • Event
    proteinuria
    Reports
    1,635
    Reporting signal score
    3,329.76
  • Event
    suspected transmission of an infectious agent via product
    Reports
    241
    Reporting signal score
    720.203
  • Event
    thrombocytopenia
    Reports
    1,584
    Reporting signal score
    714.877

And 1,494 more, listed on the interactive page.

Dose
5 mg/kg or 10 mg/kg or 15 mg/kg
Route
Intravenous
How often
Every 2 weeks or every 3 weeks

Conditions of use

  • Administer as an intravenous infusion

Prodrug
No
Chirality
Single enantiomer
Inorganic
No
Natural product
No

  • Component
    Sequence
    Type
    Protein
    Sequence
    EVQLVESGGGLVQPGGSLRLSCAASGYTFTNYGMNWVRQAPGKGLEWVGWINTYTGEPTYAADFKRRFTFSLDTSKSTAYLQMNSLRAEDTAVYYCAKYPHYYGSSHWYFDVWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHT
  • Component
    Light chain
    Type
    Protein
    Sequence
    DIQMTQSPSSLSASVGDRVTITCSASQDISNYLNWYQQKPGKAPKVLIYFTSSLHSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQYSTVPWTFGQGTKVEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC

  • 0069-0315
  • 0069-0342
  • 50242-060
  • 50242-061
  • 55513-206
  • 55513-207
  • 72606-011
  • 72606-012
  • 82491-025
  • 83257-009
  • 83257-010
  • 70121-1754
  • 70121-1755
  • 85006-1754
  • 85006-1755

Related records

Trials (2,821)

Approved for (30)

In development for (190)

Other linked conditions (7)

Targets (1)