PledPharma to close POLAR phase 3 program in the third quarter

Early in March, PledPharma decided to place recruitment and dosing of patients in the POLAR program on hold. The decision followed interactions with the French regulatory authority, ANSM, and the clinical hold issued by the US Food and Drug Administration (FDA) earlier in the year and was due to a few numbers of observed CNS related adverse events. PledPharma maintain its position that these events are not related to PledOx, a position which is also supported by the DSMB and an additional independent external evaluation of these cases. However, in a meeting in March, the independent Drug Safety Monitoring Board (DSMB) for the POLAR program recommended that the program should be stopped due to a number of severe allergic reactions observed after repeated dosing.

“Allergic hypersensitivity reactions are not uncommon in relation to platinum-based chemotherapy. However, the DSMB recommendation implies that there is an increased risk in subjects treated with PledOx. We are currently working to better understand why these allergic hypersensitivity reactions occur with coadministration of oxaliplatin and why they occur after repeated dosing.”, said Chief Medical Officer Stefan Carlsson, M.D., Ph.D.

Patients currently enrolled in the POLAR program will continue with their scheduled study procedures, while not receiving the study drug, until the data cut-off targeted in the third quarter. The POLAR program with PledOx, developed to reduce nerve damage associated with chemotherapy, consists of two studies, POLAR-A and POLAR-M, with the aim of randomizing 700 patients. POLAR-A is conducted in patients undergoing adjuvant chemotherapy treatment for colorectal cancer and was fully recruited in December 2019. POLAR-M is conducted in patients undergoing chemotherapy treatment for metastatic colorectal cancer and is not fully recruited. A total of 590 patients have been randomized in the POLAR program, of which 420 have completed more than six cycles of treatment and about 250 subjects have completed more than nine cycles. Taken together, this data will enable a robust efficacy and safety evaluation and an assessment of the benefit/risk of PledOx to evaluate if further activities to find a path forward for PledOx to treat nerve damage associated with chemotherapy are motivated.

The continuation of the development program with Aladote, developed to reduce liver damage caused by paracetamol poisoning, is not affected by the DSMB recommendation and the early closure of the POLAR program. Aladote is administered as a single dose after which severe allergic-hypersensitivity reactions have not been observed in the POLAR program. A Phase I/IIa Proof-of-Principle study has been successfully completed. A pivotal phase II/III study is under planning.

“The safety of patients in our clinical studies is our most important responsibility. Of course, the early closure of the POLAR program is a major setback for us. We will now concentrate on collecting the remaining data in the challenging COVID-19 environment and how we can best use the robust data from the POLAR studies to potentially support future clinical trials, as we believe nerve damage associated with chemotherapy remains an unmet medical need. The focus on Aladote and the forthcoming regulatory interactions and clinical study remains. For Aladote, it is reassuring that no severe allergic-hypersensitivity reactions have been observed after single dose administration”, said Nicklas Westerholm, Chief Executive Officer and President, PledPharma.

In order to continue the development of its clinical portfolio, PledPharma is well financed with approximately 255 million SEK in cash and cash equivalents reported at year end 2019.

PledPharma will host a telephone conference on April 6, 2020, at 14.00 CET.
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