(Reuters) - New data showing an experimental AstraZeneca (AZN.L) lung cancer drug shrank tumors in more than half of patients gave the British group fresh ammunition to argue that Pfizer’s (PFE.N) takeover offer undervalues it substantially.
Britain’s second-biggest drugmaker said on Thursday the strong results were among a raft of recent updates that showed accelerating progress in its pipeline of experimental medicines.
AstraZeneca has rejected a $106 billion approach from U.S. rival Pfizer, arguing that it has a bright independent future due to its promising line-up of new drugs. Pfizer is widely expected to return with a sweetened offer in coming days.
“We continue to build our pipeline and we are encouraged by the progress in the development of key assets,” Chief Executive Pascal Soriot said in a statement.
Its new lung cancer drug, known as AZD9291, targets a genetic mutation that helps tumors evade current treatments. AstraZeneca believes it could sell as much as $3 billion a year.
Results from an early-stage Phase I trial of the drug, released late on Wednesday, showed AZD9291 shrank tumors in 51 percent of patients. Tumors shrank in 64 percent of patients found to have the mutation, known as T790M, which develops in about half of lung cancers that become resistant to drugs known as epidermal growth factor receptor (EGFR) inhibitors.
Savvas Neophytou, an analyst at brokerage Panmure Gordon, said the results were impressive and “AstraZeneca’s management is right to be excited by the pipeline”.
AstraZeneca shares were 0.8 percent higher in slightly lower London market by 1400 GMT.
EGFR drugs, such as Roche’s ROG.VX Tarceva and AstraZeneca’s own Iressa, are used to treat various solid tumor cancers with mutated or overactive EGFR. Around 15 percent of patients with non-small cell lung cancer, the most common form of the disease, have mutations in the EGFR gene.
But most of them will eventually become resistant to available EGFR inhibitors, said Dr Pasi Janne, professor of medicine at Dana-Farber Cancer Institute and Harvard Medical School in Boston and the study’s lead investigator.
“The issue of drug resistance has been the bane of chemotherapy treatment of cancer for decades,” Dr Peter Yu, president-elect of the American Society of Clinical Oncology (ASCO), said during a press conference.
AZD9291 is one of several new drugs flagged by AstraZeneca last week in a bid to convince investors of the strength of its experimental pipeline, which includes several innovative cancer drugs, as well as treatments for diabetes, asthma, rheumatoid arthritis and psoriasis.
Overall, the British company forecasts these new products will help its sales rise 75 percent to $45 billion by 2023.
The Phase I trial for AZD9291, featured ahead of the annual ASCO meeting later this month, involved 199 patients with advanced non-small cell lung cancer with EGFR mutations whose disease worsened despite treatment with a current EGFR drug.
The most common side effects seen in the trial included diarrhea and rash, but researchers said the level of toxicity was less severe than is seen with available EGFR inhibitors.
AstraZeneca is currently conducting a Phase 2 study of AZD9291 in patients with the T790M mutation at a daily dose of 80 milligram, which it said could enable accelerated regulatory filing in the second half of next year.
AZD9291 has been granted “breakthrough” status by the U.S. Food and Drug Administration as a second-line therapy for non-small cell lung cancer. AstraZeneca will also study the drug as an initial treatment for eligible lung cancer patients.
Investors are keen to get a look at other cancer data from AstraZeneca due to be presented at the ASCO meeting.
The company’s MEDI4736 has the potential to become one of the first in a new class of drugs known as anti-PDL1 treatments that fight cancer by boosting the immune system. It is initially being tested as a treatment for non-small cell lung cancer and AstraZeneca said data to date had shown “durable clinical activity and acceptable safety”.
AstraZeneca has forecast potential peak sales for MEDI4736 of $6.5 billion, including combination therapies.
An AstraZeneca spokeswoman said updated data from trials of MEDI4736 will be presented at the conference at the end of May.
Data from another of the company’s experimental cancer drugs, olaparib for ovarian cancer, will be featured at the ASCO meeting. AstraZeneca has forecast peak olaparib sales of $2 billion, compared with consensus analyst estimates of $1.5 billion to $3 billion.
It has also had encouraging results combining olaparib and another drug called cediranib.
Editing by Tom Pfeiffer and Erica Billingham