Immunology

Adocia (Euronext Paris : FR0011184241 - ADOC) announces today positive final results for the first clinical trial on its innovative formulation combining insulin analog glargine (Lantus^(R), Sanofi), the gold standard basal insulin, with a rapid-acting insulin analog, lispro (Humalog^(R), Eli Lilly) using Adocia's BioChaperone^(R) technology.

BioChaperone technology enables the solubilization of insulin glargine at physiological pH, which allows its combination in solution with prandial insulins analogs such as lispro. Eight patent applications have been filed to protect this innovation until 2032.

The objective of this trial was to compare the Pharmacodynamics (PD) and Pharmacokinetics (PK) of the BioChaperone Combo with a premix formulation of an insulin analog (Humalog^(R) Mix, lispro and protamine, Eli Lilly).

Clinical results

In this double-blind crossover study, the PK/PD characteristics of BioChaperone Combo (insulin glargine 75 per cent and insulin lispro 25 per cent) were investigated. Twenty people with type I diabetes received single 0.8 U/kg doses of BioChaperone Combo and Humalog Mix25 under automated euglycemic clamp conditions (ClampArt^(R), target blood glucose (BG) 100 mg/dL, clamp duration 30 h post-dosing).

Both formulations were well tolerated and did not induce any local reaction.

BioChaperone Combo had a faster onset of action (25 plus-minus 11 vs. 40 plus-minus 13 min; p equals 0.002) and a higher early metabolic effect (AUC_GIR[0-2h] 504 plus-minus 210 vs. 325 plus-minus 183 mg/kg; p equals 0.001). The study also demonstrates a stronger late metabolic effect (AUC_GIR[12-30h] 1480 plus-minus 900 vs. 961 plus-minus 553 mg/kg; p equals 0.026) and a longer duration of action. Indeed, 30 hours after administration, 17 of the 19 patients treated with BioChaperone Combo were still under glucose control vs. only 6 of the 20 with Humalog Mix (p equals 0.0002). In summary, significant difference was observed for all these comparisons (p is less than 0.05).

PK parameters are consistent with PD and will be submitted for communication to the 74th scientific sessions of the American Diabetes Association (ADA) and the 50th European Association for the Study of Diabetes (EASD) annual meeting.

In conclusion, the clinical results demonstrate a faster prandial phase and longer basal action for BioChaperone Combo vs. Humalog Mix; indicating a better control of blood glucose. 

“We are very pleased with the final analysis of the performance of our BioChaperone Combo. There is strong evidence of the superiority of this innovative formulation to Humalog Mix, with a statistical difference for all key parameters. What is remarkable in these results is not only that the action of our Combo lasts more than 30 hours, but also, it acts more rapidly,” says Olivier Soula, deputy general manager of Adocia. 

“Based on these results, BioChaperone Combo could be a single daily injection treatment. This treatment simplification would be an important advantage for patients who currently require at least two injections per day of premix, or one of Lantus plus at least one of a fast-acting insulin,” adds Dr Tim Heise, medical doctor, CEO of Profil.

BioChaperone Combo, combining simplicity and medical performance

Today, diabetic patients who cannot control their glycemia with basal insulin alone need to add prandial insulin to their treatment. They have two options: to use either one insulin analog premix product or two insulin products, one basal and one prandial.

Premix consists in protamine precipitated (basal fraction) and soluble (prandial fraction) insulin. It eases patient life with a single product to use but it requires two injections per day to cover the patient’s basal insulin needs. The market for insulin analog premixes was worth approximately USD 2.4 billion in 2013, with USD 1.8 billion sales of NovoLog^(R) Mix (Novo Nordisk) and estimated USD 0.6 billion sales of Humalog Mix (Eli Lilly).