Drug (brand)
|
Company
|
Properties
|
Indication
|
Review
|
Alogliptin (Nesina)
|
Takeda
|
DPP4 inhibitor
|
Type 2 diabetes
|
S
|
Mipomersen (Kynamro)
|
Genzyme
|
Oligonucleotide inhibitor of apolipoprotein B100 synthesis
|
Homozygous familial hypercholesterol-aemia
|
S, O
|
Pomalidomide (Pomalyst)
|
Celgene
|
Immunomodulatory antineoplastic agent
|
Multiple myeloma
|
S, O
|
Ado-trastuzumab emtansine (Kadcyla)*
|
Genentech
|
HER2 targeted antibody and microtubule inhibitor conjugate
|
HER2 positive metastatic breast cancer
|
P
|
Ospemifene (Osphena)
|
Shionogi
|
Oestrogen receptor modulator
|
Moderate to severe dyspareunia due to menopause
|
S
|
Technetium TC 99m tilmanocept (Lymphoseek kit)
|
Navidea
|
Radioactive diagnostic agent
|
Lymphatic mapping in patients with breast cancer or melanoma
|
S
|
Gadoterate meglumine (Dotarem)
|
Guerbet
|
Gadolinium-based contrast agent
|
Contrast agent to visualize disruption of the blood–brain barrier
|
P
|
Dimethyl fumarate (Tecfidera)
|
Biogen Idec
|
MOA unknown; activates NRF2 pathway
|
Relapsing forms of multiple sclerosis
|
S
|
Canagliflozin (Invokana)
|
Janssen
|
SGLT2 inhibitor
|
Type 2 diabetes
|
S
|
Fluticasone; vilanterol (Breo Ellipta)
|
GSK
|
Corticosteroid plus LABA
|
Chronic obstructive pulmonary disease
|
S
|
Radium RA 223 dichloride (Xofigo)
|
Bayer
|
Alpha particle-emitting radioactive therapeutic
|
Castration-resistant prostate cancer
|
P
|
Dabrafenib (Tafinlar)
|
GSK
|
Kinase inhibitor with activity against BRAFV600E, BRAFV600K, BRAFV600D, wild-type BRAF and other kinases
|
Unresectable or metastatic melanoma with BRAFV600E mutation as detected by an FDA-approved test
|
S, O
|
Trametinib (Mekinist)
|
GSK
|
MEK1 and MEK2 kinase inhibitor
|
Unresectable or metastatic melanoma with BRAFV600E mutation as detected by an FDA-approved test
|
S, O
|
Afatinib (Gilotrif)
|
Boehringer Ingelheim
|
EGFR (ERBB1), HER2 (ERBB2), and HER4 (ERRB4) kinase inhibitor
|
First-line treatment of patients with metastatic NSCLC whose tumours have EGFR exon 19 deletions or exon 21 (L858R) substitution mutations as detected by an FDA-approved test
|
P, O
|
Dolutegravir (Tivicay)
|
ViiV
|
HIV1 integrase strand transfer inhibitor
|
HIV1 infection in adults and children, in combination with other antiretroviral agents
|
P
|
Vortioxetine (Brintellix)
|
Takeda
|
Serotonin reuptake inhibitor
|
Major depressive disorder
|
S
|
Bazedoxifene acetate plus oestrogens (Duavee)
|
Pfizer
|
Conjugated oestrogens with an oestrogen receptor modulator
|
Moderate to severe vasomotor symptoms associated with menopause and prevention of postmenopausal osteoporosis
|
S
|
Riociguat (Adempas)
|
Bayer
|
Soluble guanylyl cyclase stimulator
|
Persistent or recurrent chronic thromboembolic pulmonary hypertension and pulmonary arterial hypertension
|
P, O
|
Macitentan (Opsumit)
|
Actelion
|
Endothelin receptor antagonist
|
Pulmonary arterial hypertension
|
S, O
|
Flutemetamol F-18 (Vizamyl)
|
GE Healthcare
|
Radioactive diagnostic agent
|
PET imaging of the brain to estimate β-amyloid neuritic plaque density in patients who are being evaluated for Alzheimer’s disease
|
S
|
Obinutuzumab (Gazyva)*
|
Genentech
|
Humanized CD20 specific monoclonal antibody
|
Previously untreated chronic lymphocytic leukaemia
|
P, O, B
|
Eslicarbazepine (Aptiom)
|
Sunovion
|
MOA unknown, but thought to involve voltage-gated sodium channels
|
Partial-onset seizures
|
S
|
Ibrutinib (Imbruvica)
|
Pharma-cyclics
|
Bruton’s tyrosine kinase inhibitor
|
Mantle cell lymphoma
|
P, O, B
|
Luliconazole (Luzu)
|
Medicis
|
Azole antifungal
|
Interdigital tinea pedis, tinea cruris and tinea corporis caused by Trichophyton rubrum
|