AZ News from the Street 2018

More bad news in Cancer Clinical Trials:

https://www.fiercebiotech.com/biotech/astrazeneca-s-tremelimumab-fails-another-phase-3-cancer-trial

AstraZeneca’s tremelimumab fails another phase 3 cancer trial
by Nick Paul Taylor |
Dec 7, 2018 7:49am

AstraZeneca’s tremelimumab has come up short in another phase 3 trial. Having failed to improve outcomes in metastatic non-small cell lung cancer (NSCLC), the anti-CTLA4 antibody has now missed the primary endpoint in a phase 3 advanced head and neck cancer trial.

After ceding a head start to Bristol-Myers Squibb and Merck in the PD-1/PD-L1 space, AstraZeneca looked to a dual checkpoint blockade approach featuring tremelimumab to help it carve out a piece of the immuno-oncology market. The strategy was underpinned by a belief that blocking CTLA4 and PD-1/PD-L1 would yield better outcomes than monotherapies against either target in isolation.

The dual blockade approach has brought some success for Bristol-Myers, which has picked up FDA nods for its Opdivo-Yervoy combination in melanoma, renal cell carcinoma and metastatic colorectal cancer. AstraZeneca’s dual blockade program has hit some bumps in the road, though.

The latest setback comes from a phase 3 trial in patients with recurrent or metastatic head and neck squamous cell carcinoma who had progressed following platinum-based chemotherapy. Participants in the trial received either Imfinzi, the anti-PD-L1 antibody in combination with tremelimumab or standard of care chemotherapy.

Neither the Imfinzi monotherapy nor the tremelimumab combination resulted in a longer overall survival than was achieved by standard of care chemotherapy, resulting in the clinical trial missing its primary endpoint. The failure dents AstraZeneca’s hopes of bringing tremelimumab to market in head and neck cancer, but there remains a chance other data will revitalize the strategy.

“We look forward to seeing the results of the phase 3 Kestrel trial of Imfinzi and tremelimumab in patients who have not received prior chemotherapy for recurrent or metastatic head and neck squamous cell carcinoma in the first half of 2019,” AstraZeneca Chief Medical Officer Sean Bohen said in a statement.

Kestrel is one of a clutch of ongoing clinical trials that will dictate whether tremelimumab has a future. AstraZeneca is assessing the anti-CTLA4 antibody together with Imfinzi as a first-line therapy in NSCLC in two phase 3 trials and is running late-phase studies of the combination in other diseases including hepatocellular carcinoma, urothelial cancer and small-cell lung cancer.

The breadth of the late-phase program means AstraZeneca still has plenty of chances to deliver the data it needs to get tremelimumab to market. But the phase 3 data generated so far give little cause for optimism. If anything, tremelimumab looked to hinder, not help, Imfinzi in the Mystic NSCLC trial, and has now added advanced head and neck cancer trial to its list of late-phase failures.
 




more:

AstraZeneca's Imfinzi fails to meet main goals in head and neck cancer study

(Reuters) - AstraZeneca Plc's (AZN.L) immunotherapy treatment Imfinzi did not meet the main goals in a late-stage study for advanced head and neck cancer, the London-listed drugmaker said on Friday.

The study, known as "EAGLE", did not improve overall survival compared with standard chemotherapy in patients with the hard-to-treat disease, the company said.

The results come after AstraZeneca warned last month that its immunotherapy treatment Imfinzi did not meet the main goal of improving survival rates for patients with the most advanced form of lung cancer, putting pressure on its shares.

AstraZeneca has been seen as having a head start in the race for cancer treatments, and Imfinzi was aiming to be the new standard of care in treating early inoperable stage III lung cancer.

"While these results are disappointing, we remain committed to evaluating the potential of Imfinzi and other innovative medicines for patients with head and neck cancer," said Chief Medical Officer Sean Bohen.

The trial was conducted at 169 centres across 24 countries including the U.S., Europe, South America, Japan, Korea, Taiwan, Israel and Australia, AstraZeneca said.
 




Another big competitor will probably enter the PARP market with the takeover of a small one:

Clovis Oncology Inc (NASDAQ: CLVS) has emerged as a strong takeover candidate following GlaxoSmithKline plc (NYSE: GSK)'s proposed acquisition of TESARO Inc (NASDAQ: TSRO), according to Gabelli Research.

Merck & Co., Inc. (NYSE: MRK)'s $5-billion purchase of half of the commercial rights of AstraZeneca plc (NYSE: AZN)'s Lynparza in 2017 leave Clovis as the sole standalone PARP oncology company, giving it a scarcity value, analyst He said in a Tuesday note. (See his track record here.)

Bristol-Myers Squibb Co (NYSE: BMY), Novartis AG (NYSE: NVS)' Sanofi and Roche Holdings AG Basel ADR Common Stock (OTC: RHHBY) among the potential suitors, the analyst said.

Clovis' Rubraca — a PARP inhibitor — is being evaluated in combination with Bristol-Myers' Opdivo as a first-line maintenance therapy for ovarian cancer in the ATHENA trial, He said. Data from the trial is expected in early 2021.

Although Clovis is behind the AstraZeneca-Merck combine and Tesaro-GSK in development, Clovis is in a better long-term position due to data generated by the Rubraca-Opdivo combination, He said.

Clovis is evaluating Rubraca as monotherapy to treat prostate cancer in TRITON2 and TRITON3 trials, thr

The company looks forward to filing application to the FDA by year-end 2019, the analyst said.

Gabelli views data updates from TRITON2/3 trials at the ASCO meeting in June as the next catalysts for Clovis shares.
 




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