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Peregrine Pharmaceuticals, Inc. Message Board

  • r2_d2_l80 r2_d2_l80 Feb 26, 2013 9:15 AM Flag


    Peregrine Pharmaceuticals' Bavituximab: It's Time To Throw In The Towel
    Feb 26 2013, 05:49 | 1 comment | about: PPHM
    Disclosure: I have no positions in any stocks mentioned, and no plans to initiate any positions within the next 72 hours. (More...)

    Peregrine Pharmaceuticals, Inc. (PPHM) was formed more than 30 years ago and has never been profitable. Their lead asset, bavituximab, has been in development since 2005; 735 patients have been treated in 16 trials and there is currently no visible path to registration. Despite the doom and gloom, Peregrine's top five executives feel justified in rewarding themselves with nearly $3MM/year in compensation; so much for pay for performance.

    Bavituximab, a first-in-class phosphatidylserine-targeting chimeric antibody (having mouse and human components), is the centerpiece of Peregrine's pipeline. Phosphatidylserine (PS) is a phospholipid that is expressed on the surface of many cancer cells and cells undergoing apoptosis making it a logical target for cancer therapy.

    Clinical development of bavituximab for the treatment of cancer began in 2008. Since that time, Peregrine has conducted twelve Phase-I/-II studies and treated 613 cancer patients but has yet to observe a statistically significant improvement over a contemporary standard-of-care (SOC).

    Lung Cancer

    Peregrine initiated a randomized Phase-II study of docetaxel ± bavituximab in 2nd-line NSCLC patients (N=121) in 2010. The results of the study were the subject of a recent press release in which the company reported that the "results from this Phase-II trial indicate a meaningful improvement in median overall survival of 11.7 months in the 3mg/kg bavituximab plus docetaxel arm compared to 7.3 months in the control arm (HR=0.73; p value=0.217)." To add to the hype, the company went on to say that "these compelling results strongly support advancing the 3mg/kg bavituximab plus docetaxel combination into Phase-III development in second-line NSCLC." To be clear, this was a failed trial (P = 0.217), the results were not compelling and the "improvement" in median overall survival was orders of magnitude away from achieving statistical significance. This was, in part, due to the inclusion of a 1 mg/kg dose arm which reduced the size of each arm to 40 patients. Given that there was a significant volume of data available for docetaxel in combination with 3mg/kg of bavituximab at the time this study was initiated, there was no apparent reason to include the 1mg/kg arm.

    Based on the results of a Phase-II study (NCT00687817) with bavituximab in combination with paclitaxel and carboplatin in previously untreated NSCLC patients (N=49), the company initiated a randomized Phase-II study with carboplatin/paclitaxel ± bavituximab (NCT01160601) in the same patient population (N=86). It is disappointing that the company chose to limit this study to 86 patients as it will be difficult to "tease out" differences between the arms of the study. Clinical development is more than simply conducting clinical trials, it's about asking hard questions and designing and conducting clinical trials to secure definitive answers. Regrettably, this study, which should read out shortly, is underpowered and not designed to provide definitive answers.

    Another Peregrine study in NSCLC that will not likely advance the development of bavituximab is study NCT01323062, in which the safety and efficacy of bavituximab in combination with pemetrexed (Alimta®) and carboplatin in previously untreated patients (N=25) is being evaluated. It is not clear what the company had in mind when designing this trial as pemetrexed is only approved for use in combination with cisplatin


    In reviewing the development history of bavituximab it is difficult to understand the rationale for much of what Peregrine has done; specifically, the large number of open-label studies, the small number of randomized studies and the fact that the randomized trials were underpowered. Moreover, the company has not provided statistical information (e.g., power to detect differences of a stated magnitude) for any of its randomized trials leading one to wonder if the trials were so underpowered that the company was uncomfortable sharing this information. Then there are the results from the failed randomized trials in 2nd-line NSCLC and 1st-line pancreatic cancer which have seemingly been ignored by the company. Finally, the development history of bavituximab suggests reluctance on Peregrine's part to test the drug in a well-powered study. The party is over for Peregrine, investors are losing patience and it's time to move on.

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