Background

Intestinal nematode infections are commonly diagnosed in dogs from all parts of the world, including Europe [1,2,3,4]. Of these intestinal nematodes, Ancylostoma caninum and Toxocara canis are considered two of the most important and commonly reported helminth parasites of dogs [5, 6]. Dogs infected with A. caninum hookworm can play an important role in the transmission of this potentially zoonotic nematode by excreting eggs directly into the environment where humans and other dogs can be subsequently exposed to infective larvae. The veterinary and public health aspects of hookworm infections in dogs are well established [5]. In Europe, A. caninum and Uncinaria stenocephala are two hookworm species routinely found in dogs; however, A. caninum is reported to be found predominantly in dogs located in southern Europe [7].

Endectocidal combination products or anthelmintics with a broad spectrum of activity can provide the pet owner and veterinarian with the ability to treat dogs that are concurrently infested or infected with multiple parasite types. As reported herein, the combination of milbemycin oxime (MO) and lotilaner is one such example. The effectiveness of MO in combination with other drug substances administered to dogs that were naturally infected with different species of adult intestinal nematodes has been previously demonstrated in laboratory dose confirmation studies [8]. Additionally, it has been shown that a minimum dosage of 0.75 mg/kg of MO will prevent the establishment of the adult stage of the French heartworm, Angiostrongylus vasorum, and larval and immature adult stages of T. canis and A. caninum [9, 10]. The second drug substance in this fixed combination, lotilaner, has demonstrated excellent effectiveness against several ectoparasites (i.e., fleas, ticks, mites) on dogs [11,12,13,14,15,16,17,18,19,20,21,22,23,24].

The objective of both dose confirmation studies as summarized herein was to confirm the dose and non-interference of lotilaner (alone or in combination) with milbemycin oxime and to evaluate the effectiveness when administered at approximately the lower end (0.75 to 1.11 mg/kg MO) of the proposed MO tablet unit dose range (0.75 to 1.53 mg/kg MO), in dogs experimentally infected with immature (L4 and immature adult [L5]) stages of Ancylostoma caninum.

Methods

Use of the lotilaner and MO combination investigational product (IP) in this study was intended to evaluate a proposed commercial formulation and dose regimen for use in dogs under end-user conditions for the intended European and global intestinal nematode label indications. As such, both dose confirmation studies were negative-controlled, masked, randomized laboratory studies to evaluate the effectiveness and safety of a combination of lotilaner and MO chewable tablets (IP) administered orally to dogs experimentally inoculated with A. caninum. These studies were conducted in accordance with the principles of GCP as laid down in the VICH guidelines GL9, Good Clinical Practice (June 2000); The Efficacy Requirements for Anthelmintics: Overall Guidelines (VICH GL7); The World Association for the Advancement of Veterinary Parasitology (WAAVP) guidelines for evaluating the efficacy of anthelmintics for dog and cats; VICH GLl9 Effectiveness of Anthelmintic and Overall Guidelines: Specific Recommendation for Canines (June 2001) [25,26,27,28]. Study site personnel involved in making assessments of intestinal nematode effectiveness and safety were masked to treatment assignments.

Animals

In both studies purpose-bred laboratory research beagles were sourced from a USDA licensed vendor. All dogs were confirmed upon arrival to be free of any intestinal nematodes. These dogs were a mix of male/female, 2–3 months of age when inoculated with hookworm third-stage (L3) infective larvae, and had a body weight range of 3.65–7.0 kg. All dogs were acclimated for a minimum of 14 days prior to inoculation with infective L3 stages of A. caninum on day 0. All dogs were singly housed throughout the study in concrete floored pens that were cleaned daily and that restricted contact between dogs in adjacent pens, they were fed a balanced commercial dry dog food daily and provided with water ad libitum. Dogs were individually identified by ear tattoo. Physical examinations were performed during the acclimation period to ensure dogs were healthy and were eligible to be enrolled into each study. After day 0, all enrolled dogs were examined at least once daily for any abnormal clinical signs or adverse events. The primary inclusion criterion was body weight so that each selected dog fell into a defined weight range in order to ensure that dogs were dosed with whole tablet(s) to deliver between 0.75 and 1.11 mg/kg of MO, which is the approximate lower half of the tablet unit dose range. In study 1, 51 dogs and in study 2, 44 dogs were orally inoculated with approximately 300 infective A. caninum L3 once on day 0. All dogs that met the inclusion/exclusion criteria were weighed on day 6 and then randomized to one of the six (study 1) or four (study 2) treatment groups.

Experimental hookworm inoculations

On day 0 of each study, dogs were inoculated with 300 infective L3 of A. caninum via oral gavage. The L3s were confirmed by morphology to be those of A. caninum. All dogs within each study were inoculated orally using the same inoculation method. Any calculations needed to determine inoculum volume were recorded. Dogs were checked for vomiting at 1 h ± 30 min post-inoculation. The A. caninum isolate used in each study (separate isolate for each study) was a field strain and had undergone zero passages. Each isolate used at each study site was sourced from a local naturally infected dog accessed by each USA study site.

Randomization and treatment

All dogs were weighed using certified scales on the day before the scheduled treatment to confirm eligibility within protocol defined weight ranges. Eligible dogs were then randomized into the treatment groups in a completely randomized design.

All dogs were fed a small portion of a moist canned food just prior to their scheduled dosing time point. Treatments using the intended commercial solid oral dosing formulation (Credelio Plus; Elanco Animal Health) were administered in a time frame relative to inoculation so that effectiveness could be assessed primarily against immature larval (L4) or immature adult [L5] stages of A. caninum. Dogs were orally treated with whole tablets by pilling with the MO + lotilaner combination tablets on day 7 (to assess efficacy against L4 stages based on the life cycle) or on day 11 (to assess efficacy against immature adults [L5] based on the life cycle). All corresponding control groups received a vehicle control tablet on day 7 or day 11. In study 1, an additional treatment group was included using lotilaner as a mono product (Credelio™) and was administered to dogs on day 7 or day 11 to assess non-interference. Treatment day dog observations were performed just after dosing on each scheduled dosing day and at 1 and 2 h as well as 4 and 8 h to confirm that the oral solid dosing formulation had been accepted and that any abnormal health observations were documented.

Necropsy/worm counts

All dogs treated on day 7 or 11 were euthanized and necropsied 5 days post-treatment in accordance with relevant laboratory procedures. Food was removed for an overnight fast the day prior to each scheduled necropsy date. The entire digestive tract was removed and processed in accordance with the relevant standard operating procedures of each study site and standard parasitological procedures. Since immature stages of A. caninum were being assessed, the intestinal contents were washed over a fine mesh sieve (#100; 0.15 mm aperture). Additionally, the small intestine was soaked for approximately 2 h in warm saline to facilitate the emergence of immature stages from mucosal tissues. Materials recovered from soaked intestines were similarly sieved for worm recovery. The worms recovered from each dog were preserved in 10% formalin prior to being counted and microscopically identified to species and stage.

Variable classification

The primary variable evaluated was the total count of adult, immature L4 and immature adult stages of A. caninum recovered at each post-treatment necropsy day. Each treatment was administered in a time frame relative to inoculation so that effectiveness could be assessed primarily against immature L4 or immature adult stages of A. caninum. Efficacy against experimentally induced A. caninum populations was determined post-treatment for the MO + lotilaner combination or the lotilaner mono product by comparing the geometric mean total count with that in the corresponding vehicle control group. Based on the time interval between dosing and when dogs in each group were necropsied, for the L4 group, immature adults were expected to be present and adults would be present for the immature adult (L5) group based on the pre-patent period of A. caninum. Efficacy ≥ 90% and a statistically significant difference (P < 0.05, two-sided) between each vehicle control group and the corresponding MO + lotilaner treated groups was required to demonstrate effectiveness in the MO + lotilaner treated groups against the L4 or immature adult stages of A. caninum. As per VICH guidelines, a minimum of five specimens of any stage (total of immature L4, immature adult, mature adult) was required in a minimum of six control dogs at the end of each study to meet adequacy of infection criteria for each parasite stage of interest.

Data analysis

For each dog the total A. caninum counts at necropsy were calculated as the sum of the immature L4, immature adult and adult counts. A logarithmic transformation (ln[count + 1]) was applied to the total post-treatment worm count for each individual animal to address the skewed nature of these data and also to allow zero counts. Back-transformed geometric means (GM) were calculated as (emean – 1) where the "mean" was the treatment group arithmetic mean of log-transformed counts at a given time point. The efficacy against each stage of A. caninum was calculated using the following formula: [(C − T)/C] × 100, where C was the geometric mean total worm count for the placebo group and T was the geometric mean total worm count for the treated group. The transformed counts were analyzed with a general linear model with fixed effect treatment and block as a random effect. In order to assess the effectiveness of the treatment against the immature L4 stage of A. caninum, statistical contrasts were constructed comparing the L4 control group against the L4 treated group in each of the studies. Similarly in each study, the immature adult control group and the immature adult treated group were compared to determine the effectiveness of the treatment against the immature adult stage [L5] of A. caninum. All statistical analyses used the statistical package SAS 9.4 (Cary, NC).

Results

Based on daily observations to assess any adverse events, there were no mortalities and no treatment-related adverse reactions in either laboratory dose confirmation study. Effectiveness results against immature A. caninum stages are summarized in Table 1.

Table 1 Effectiveness of a single oral dose of a novel chewable tablet (Credelio Plus) containing milbemycin oxime and lotilaner against induced L4 larval and immature adult (L5) Ancylostoma caninum infections in dogs
Full size table

L4 A. caninum worm counts: study 1

All eight dogs in the vehicle control group (treated on day 7) had positive A. caninum counts recorded at necropsy with a range of 60–248 worms (Table 1). This demonstrated a robust level of infection because all 8 of the control dogs were adequately infected with at least 60 worms. The geometric mean (GM) A. caninum count for the vehicle control group was 171.9. A small number of A. caninum were recovered from all 8 dogs in the Credelio Plus group (range 1–15). The GM A. caninum count for the Credelio Plus group was 4.6. The GM A. caninum count for the Credelio (Mono) group to assess non-interference of lotilaner was 171.7 (range 98–236). The effect of the Credelio Plus tablet on L4 A. caninum was clearly demonstrated at necropsy based on worm counts and as compared to the vehicle control group. Post-treatment A. caninum worm counts were significantly different (P-value < 0.001) between the Credelio Plus group compared to the vehicle control group. Non-interference between the active ingredients was also demonstrated because the counts in the Credelio Plus group were significantly lower than in the Credelio Mono group (P < 0.001) and efficacy in the Credelio Plus group exceeded 90% while efficacy in the Credelio Mono group was < 1%.

Immature adult (L5) A. caninum worm counts: study 1

All eight dogs in the vehicle control group (treated on day 11) had positive A. caninum counts recorded at necropsy with a range of 173–255 (Table 1). This demonstrated a robust level of infection because all 8 of the control dogs were adequately infected with at least 173 worms. The GM A. caninum count for the vehicle control group was 198.7. Ancylostoma caninum were recovered from six of the eight dogs in the Credelio Plus group (range 0–86). The GM A. caninum count for the Credelio Plus group was 2.5. The GM A. caninum count for the Credelio Mono group was 178.8 (range 149–231).

The effect of the Credelio Plus tablet on immature adult (L5) A. caninum was clearly demonstrated at necropsy based on worm counts and as compared to the vehicle control group. Ancylostoma caninum worm counts were significantly reduced post-treatment from 198.7 in the vehicle control group to 2.5 in the Credelio Plus treated group (98.7% efficacy). Post-treatment A. caninum worm counts were significantly different (P-value < 0.001) between the Credelio Plus group compared to the vehicle control group. Non-interference between the active ingredients was also demonstrated because the immature adult (L5) counts in the Credelio Plus group were significantly lower than in the Credelio Mono group (P < 0.001) and efficacy in the Credelio Plus group exceeded 90% while efficacy in the Credelio Mono group was 10%.

L4 A. caninum worm counts: study 2

All 10 dogs in the vehicle control group had positive A. caninum counts recorded at necropsy with a range of 42–156 (Table 1). This demonstrated a robust level of infection because all 10 of the control dogs were adequately infected with at least 42 worms. The GM A. caninum count for the vehicle control group was 79.4. In total, four A. caninum were recovered from three of the 10 dogs (two dogs had 1 worm, and one dog had 2 worms) in the Credelio Plus group. The GM A. caninum count for the Credelio Plus group was 0.3. The effect of the Credelio Plus tablet on L4 A. caninum was clearly demonstrated at necropsy based on worm counts and as compared to the vehicle control group. Ancylostoma caninum worm counts were reduced significantly post-treatment from 79.4 in the vehicle control group to 0.3 in the Credelio Plus treated group (99.6%). Post-treatment A. caninum worm counts were significantly different (P-value < 0.001) between the Credelio Plus group compared to the vehicle control group.

Immature adult [L5] A. caninum worm counts: study 2

All 10 dogs in the vehicle control group had positive A. caninum counts recorded at necropsy with a range of 61–302 (Table 1). This demonstrated a robust level of infection because all 10 of the control dogs were adequately infected with at least 61 worms. The GM A. caninum count for the vehicle control group was 109.7. In total, six A. caninum were recovered from 2 of the 10 dogs (2 dogs with 3 worms each) in the Credelio Plus group. The GM A. caninum count for the Credelio Plus group was 0.3. The effect of the Credelio Plus tablet on the immature adult (L5) A. caninum was clearly demonstrated at necropsy based on worm counts and as compared to the vehicle control group. Ancylostoma caninum worm counts were reduced significantly from 109.7 in the vehicle control group to 0.3 in the Credelio Plus treated group (99.7%). Post-treatment A. caninum worm counts were significantly different (P-value < 0.001) between the Credelio Plus group compared to the vehicle control group.

Discussion

The objective of both dose confirmation studies was to evaluate the effectiveness and safety of Credelio Plus (lotilaner + milbemycin oxime), administered once for the treatment of immature stages of the intestinal nematode species A. caninum. The two-dose confirmation studies summarised above clearly demonstrated that the Credelio Plus chewable tablets administered orally at approximately the lower end (0.75 to 1.11 mg/kg MO) of the proposed MO tablet unit dosage range (0.75 to 1.53 mg/kg MO) was highly efficacious when treating dogs that were infected with immature (L4 and immature adult [L5]) stages of A. caninum at the time of each treatment. In studies designed to treat immature A. caninum, worm counts were reduced by 97.3% to 99.7%, in both studies in comparison to a vehicle control group.

Larval stages of A. caninum are considered the dose-limiting intestinal nematode species for MO and a minimum MO dosage of 0.75 mg/kg was confirmed in these studies to demonstrate adequate and substantial evidence of effectiveness [10]. It was previously reported that slightly lower dosages of MO at 0.5 mg/kg did not demonstrate acceptable (> 90%) efficacy against larval (L4) or immature adult stages of this pathogenic hookworm species of dogs [29]. These authors reported that 0.5 mg/kg MO had 49% efficacy against L3/L4 stages, 83% against L4 and 81% against early (immature) adult stages of A. caninum. It is very important that administered doses of MO and other anthelmintics are accurate, based on the approved label dosage (mg/kg) and the dog’s body weight, because small variations could potentially impact the overall efficacy against different life cycle stages of pathogenic parasites such as A. caninum.

The ectoparasiticidal component of the IP, lotilaner, is already registered in the European Union (lotilaner, Credelio chewable tablets for dogs) for the treatment of flea (Ctenocephalides felis and C. canis) and tick (Rhipicephalus sanguineus, Ixodes ricinus, Ixodes hexagonus, and Dermacentor reticulatus) infestations in dogs, and additionally has been shown to be effective against other global tick and mite species [11,12,13,14,15,16,17,18,19,20,21,22,23,24]. To extend the effectiveness of the commercial drug product when dogs have concurrent nematode infections and ectoparasite infestations, lotilaner was combined with MO to form Credelio Plus. Ancylostoma caninum along with other intestinal nematode species is commonly reported from dogs globally as well as in Europe [2, 5, 6, 30, 31].

Since both the larval and adult stages of A. caninum are very pathogenic in dogs and are commonly diagnosed in the general dog population, this further warrants the need to routinely conduct periodic faecal examinations and to treat dogs for this intestinal nematode parasite. This includes dogs maintained in their home environment as well as pets that contact other dogs or visit places contaminated by dog feces because these circumstances may support transmission of parasites [32, 33]. The use of Credelio Plus as a broad spectrum endectocide that pet owners and veterinarians can use to effectively treat dogs with adult and immature intestinal nematode infections supports the recommendations from scientific expert groups such as ESCCAP and TroCCAP to provide regular treatment and control of all intestinal nematodes of dogs and cats [34, 35]. If A. caninum is a concern based on past infections or exposure to contaminated areas, deworming at least four times a year should be considered if dogs and cats are housed outside or have access to the outdoors. ESCCAP further points out that the routine treatment and prevention of all intestinal parasites depends upon legislation in individual countries, veterinary professionals taking local epidemiological circumstances into account, owner perception, and individual risk assessments (e.g., hunting pets, previous lungworm exposure, raw meat diets). Deworming practices should therefore always be on the advice of a veterinary professional. The use of Credelio Plus is of particular importance for zoonotic species like T. canis and the zoonotic and pathogenic hookworm species, A. caninum. Both are commonly reported in dogs of all ages and throughout the year in prevalence studies conducted in different areas of the world, including healthy, well-cared-for dogs in Europe [3, 4, 30,31,32,33, 36, 37]. There is surprisingly little information about the impact of re-treatment intervals on parasite burdens and environmental contamination on which to base a maximum re-treatment interval. Current information suggests that annual or twice-yearly treatments do not have a significant impact on preventing patent intestinal nematode infections within a population of dogs, so a treatment frequency of at least 3–4 times per year is a general recommendation that may reduce faecal egg shedding and environmental contamination [31]. Monthly deworming treatments can largely prevent patent infections as it takes into account the biology and pre-patent period of these different intestinal nematode parasites. It was shown that the prevalence of common nematode and cestode endoparasites declined significantly in a population of well-cared for dogs in which broad spectrum endectocides were used on a monthly basis [38]. The MO minimum dosage (0.75 mg/kg) in Credelio Plus additionally has been shown to effectively treat dogs with L4 and immature adult stages of both T. canis and A. caninum and for reducing the level of infection with the lungworm, Angiostrongylus vasorum and thereby also reducing environmental contamination [9, 10].

MO, used alone or in combination with other oral parasiticides, has been used safety for over 20 years for intestinal nematode control and heartworm prevention in dogs [39]. It has however been recently documented that there are multiple-drug resistant field isolates of adult A. caninum [40]. Lotilaner (Credelio) as a stand-alone product administered as an oral ectoparasiticide has demonstrated safety for dogs under both field use and laboratory conditions [11,12,13,14,15,16,17,18,19,20,21,22,23,24].

Conclusions

These studies confirmed the efficacy of a single oral dosage of a novel, chewable tablet containing milbemycin oxime and lotilaner (Credelio Plus) against immature stages of A. caninum infections in dogs. This new combination treatment option of lotilaner + MO can be used to provide broad spectrum parasite control for dogs because it offers flea and tick prevention and control, intestinal parasite treatment and control, and heartworm and lungworm disease prevention. This will contribute to owner compliance and simplifies the treatment recommendations from global scientific groups and veterinarians to prevent or treat these parasites as well as decreasing the transmission of important zoonotic parasites and tick- and flea-transmitted disease agents.