Three triple-combination treatments fromVertexPharmaceuticalsshowed promising results in Phase 1 and Phase 2 clinical trials in cystic fibrosis (CF) patients with one F508del mutation and one so-called minimal function mutation (F508del\/Min) in the CFTR gene, the defective gene that causes CF. <\/p>\n
Vertexannounced that these are the first data to demonstrate that it is possible to treat the underlying cause of CFinpatients with these mutations, which are particularly difficult to treat. <\/p>\n
Minimal function mutations are gene changes that leave the CFTR protein minimally functional or unable to function at all. Earlier studies showed that patients with these types of mutations are not responsive to treatment withKalydeco (ivacaftor),tezacaftor, or the combination of the two. <\/p>\n
Two Phase 2 trials studied tezacaftorand Kalydecoin combination with eitherVX-440orVX-152, two investigational therapies thatare next-generation correctors of the defective CFTR protein. <\/p>\n
The trials showed that patients improved their lung function, as measured by percent predicted forced expiratory volume in 1 second(ppFEV1),and lowered the amount of chloride in their sweat, a measure of how well the CFTR protein works. <\/p>\n
A Phase 1 clinical trial explored atriple combination with VX-659, which is another corrector.This study showed similar improvements in lung function and sweat chloride analyses. <\/p>\n
The trials showed thatall of the treatmentswererelatively safe, with the majority of adverse events being mild or moderate. <\/p>\n
These safety and efficacy data are clear and compelling, indicating significant potential benefit for people with CF from each of these three different triple combination regimens, Jeffrey Chodakewitz, MD, executive vice president and chief medical officer at Vertex, said in apress release. <\/p>\n
We will be collecting and evaluating additional data from these and other studies and will make a decision on which regimen(s) to take forward intopivotalprogram(s), which we expect to begin in the first half of 2018, Chodakewitz added. <\/p>\n
The Phase 2 study (NCT02951182) is evaluating two doses of VX-440 200 mg and 600 mg every 12 hours in combination withtezacaftorand Kalydeco.The trial includes adult patients who have either two F508del mutations or the F508del\/Min combination of mutations. <\/p>\n
Among 47 patients with minimal function mutations analyzed so far, the average lung function was found to be improved by about 10-12%. Meanwhile, theamount of chloride in patients sweat decreased, indicating improved activity of the CFTR protein. <\/p>\n
Researchers noted both of these positive effects in both dose groups (200 and 600 mg). In contrast, those who received a placebo had no changes in these parameters during four weeks of treatment. <\/p>\n
The treatment was also beneficial to26 patients with two F508del mutations who were already receiving treatmentwith the tezacaftor-Kalydeco combo. These patients were randomized to receive either VX-440 or a placebo for four weeks. <\/p>\n
Like the other patient group, the addition of VX-440 to the treatment plan improved lung function by 9.5%. It also significantly lowered sweat chloride levels. <\/p>\n
A second Phase 2 trial (NCT02951195) studied three doses of VX-152 100 mg, 200 mg, and 300 mg every 12 hours together withtezacaftorand Kalydeco. Patients are adults with either two F508del mutations ora F508del\/Minmutation combination. <\/p>\n
In patients withF508del\/Min mutations, two weeks of treatment allowed those in the lower dose group to improve by 5.6% on lung function tests, while those in the higher group improved by 9.7%. Sweat chloride levels also decreased in this study. <\/p>\n
A similar result was observed in patients with two F508del mutations: 7.3% improvement in lung function and a decrease in sweat chloride levels. <\/p>\n
The Phase 1 study (NCT03029455) differs in design from the Phase 2 trials as it evaluates increasing doses of VX-659 alone and in triple combination withtezacaftorand Kalydecoin healthy volunteers. The trialalso includes patients with the F508del\/Min mutations. <\/p>\n
As in the other studies, preliminary results showed an improvement of 9.6% in patientslung functionafter two weeks of treatment. <\/p>\n
Patients with minimal function mutations have been waiting for a medicine to treat the underlying cause of their disease, which makes these data, showing pronounced improvements in lung function particularly important, said Steven M. Rowe, MD, co-chair of a steering committee of global CF experts who advise Vertex on the development of the triple combination treatments. <\/p>\n
Its also encouraging to see that the addition of a next-generation corrector may lead to substantial additional benefits for patients with two copies of the F508del mutation, who were already receivingtezacaftorand ivacaftor, added Rowe, who is also a professor of medicine, pediatrics, and cell developmental and integrative biology at theUniversity of Alabama at Birmingham. <\/p>\n
All three studies are still recruiting participants. More information and study locations can be found at the respective trial pages at these links:NCT02951182,NCT02951195, andNCT03029455. <\/p>\n
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Data From Vertex's Triple-Combination Trials Show Promising Benefits for CF Patients - Cystic Fibrosis News Today<\/a><\/p>\n","protected":false},"excerpt":{"rendered":" Three triple-combination treatments fromVertexPharmaceuticalsshowed promising results in Phase 1 and Phase 2 clinical trials in cystic fibrosis (CF) patients with one F508del mutation and one so-called minimal function mutation (F508del\/Min) in the CFTR gene, the defective gene that causes CF. Vertexannounced that these are the first data to demonstrate that it is possible to treat the underlying cause of CFinpatients with these mutations, which are particularly difficult to treat. Continue reading