Preclinical studies have demonstrated the safety of NFL-101, leading regulatory bodies to authorize its administration to humans in clinical trials.

Phase 1 (CESTO) and Phase 2a (PRECESTO) clinical studies endorsed the safety of NFL-101, and also provided the first data measuring its efficacy in a controlled environment.

Results from the Phase 2b efficacy study (CESTO 2) are expected in July 2024.

A phase 1 study, CESTO (NCT02521701), was conducted by the Montpellier Regional Cancer Institute (ICM) on 24 smokers to confirm safety. The last 12 subjects were recruited with the intention of making a quit attempt, at which point efficacy could be measured.

The safety of the product was confirmed, with the absence of side effects, and a specific action on the immune system was demonstrated.

The 24 subjects in the study described a reduction in satisfaction with cigarettes and a reduction in the desire to smoke.

Continued abstinence rates measured over the last 12 subjects are very encouraging when compared with the efficacy of current treatments:

Sources: EAGLES study for Patch nicotine and Champix®/Chantix®; ORCA-2 and ORCA-3 studies for cytisine; CESTO study for NFL-101

Reducing the satisfaction associated with smoking prior to a quit attempt weakens the link between smoking and its reward, thereby improving the success of quit attempts. Champix®/Chantix® achieves this by reducing cigarette satisfaction during the 7-10 day pre-treatment period. This contributes to its greater efficacy when compares to nicotine replacement therapies such as patches.

PRECESTO (NCT06091826) is a Phase 2a, cross-over, randomized, double-blind, exploratory clinical study, over two 28-day periods, involving 34 subjects who did not want to quit smoking, and whose aim is to measure the reduction in satisfaction provided by cigarettes.

PRECESTO shows that NFL-101 reduces smoking satisfaction. The reduction is greater than that observed with Champix®/Chantix®.

The therapeutic value of reinforcing the efficacy of current smoking cessation medications, particularly nicotine substitutes, by pretreatment with NFL-101 is confirmed.

Source: PRECESTO study; study NCT02634281 (Bohadana A, 2020)

A phase 2b study, CESTO2 (NCT04571216), multicenter (9 clinical centers in France), randomized, double-blind, placebo-controlled study involving 318 subjects is currently underway. Recruitment was completed in May 2023, and subjects will be followed up for 12 months. The primary endpoint is continuous abstinence for 4 weeks, and the secondary endpoints are continuous abstinence for longer periods of up to 12 months.

NFL-101 is administered via two subcutaneous injections, the first coinciding with the target quit date and the second one week later, facilitating compliance. Two additional optional injections are offered to subjects who have not managed to quit, or who have relapsed, at months 3 and 6.

Results expected in July 2024 will also be compared with the efficacy of currently approved or pending drugs:

Sources: EAGLES study for Patch nicotine and Champix®/Chantix®, ORCA-2 and ORCA-3 studies for cytisine

The development of NFL-101 was initiated following the observation of the efficacy of a tobacco leaf allergy desensitization treatment in smoking cessation. As is often the case with botanical drugs, understanding the mechanism of action is eventually refined during development.

The mechanism of tobacco addiction is only partially understood, and recent advances suggest that reduced microglial cell activity reinforces tobacco addiction.

As demonstrated in preclinical and Phase 1 studies, NFL-101 activates certain pro-inflammatory cytokines and IgG. There is a possible link between this immune activation and a stimulation of microglial activity, leading to a change in smoking behavior.

This hypothesis is currently being tested by the CEA, with results expected in Q1 2024.