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Investors watching for new approvals and cancer, Orphan data in 2Q17
Investors are hoping that a slew of approvals and data readouts can maintain biotech’s momentum on the heels of several high-profile successes that came just before or after 1Q’s end.
Chief among those was Vertex Pharmaceuticals Inc.’s Phase III data for the combination of tezacaftor (VX-661) and Kalydeco ivacaftor in cystic fibrosis. Tezacaftor is expected to be part of a triple combination therapy that could potentially address a wider population of CF patients than those with delta F508 mutations in the cystic fibrosis transmembrane conductance regulator (CFTR).
The doublet met the primary endpoint of an improvement in absolute percent predicted forced expiratory volume in one second (ppFEV1) in both the Phase III EVOLVE and Phase III EXPAND trials. EVOLVE enrolled patients with two copies of the delta F508 mutation, while EXPAND enrolled patients with residual CFTR function and one delta F508 mutation.
On March 29, Vertex jumped $18.34 (20%) to $108.01 after reporting the data, adding $4.6 billion in market cap.
Vertex is conducting Phase II trials of two separate triple combinations: CFTR corrector VX-440 plus tezacaftor/ivacaftor; and CFTR corrector VX-152 plus tezacaftor/ivacaftor. Data from both studies are expected next half.
OrbiMed Advisors’ Sven Borho told BioCentury, “The Vertex triple data is probably the most important of the year.”
“The Vertex triple data is probably the most important of the year.”
Two highly anticipated approvals also came just before the quarter’s end. Tesaro Inc.’s Zejula niraparib was approved three months ahead of its June 30 PDUFA date as maintenance treatment for recurrent epithelial ovarian, fallopian tube or primary peritoneal cancer following platinum-based chemotherapy.
Several investors think approval further de-risks Tesaro and increases the likelihood that the cancer company will get taken out.