Approval Date: April 10, 1997
Freedom of Information Summary
NADA 141-084
I. GENERAL INFORMATION:
NADA 141-084 Sponsor: Novartis Animal Health US, Inc.
Post Office Box 18300
Greensboro, NC 27419-8300Generic Name: milbemycin oxime/lufenuron tablets Trade Name: Sentinel™ Tablets Marketing Status: Rx: U.S. Federal law restricts this drug to use by or on the order of a licensed veterinarian II. INDICATIONS FOR USE
SENTINEL Tablets are indicated for use in dogs and puppies four weeks of age and older and two pounds body weight or greater, for the prevention of heartworm disease caused by Dirofilaria immitis, for the prevention and control of flea populations, the control of adult Ancylostoma caninum (hookworm), and the removal and control of adult Toxocara canis, Toxascaris leonina (roundworm) and Trichuris vulpis (whipworm) infections.III. DOSAGE FORM, ROUTE OF ADMINSTRATION AND RECOMMENDED DOSAGE
SENTINEL Tablets are given orally, once a month, at the recommended minimum dosage of 0.23 mg/lb (0.5 mg/kg) milbemycin and 4.55 mg/lb (10 mg/kg) lufenuron.4. Effectiveness
Recommended Dosage Schedule Milbemycin Oxime Lufenuron Body weight per Tablet per Tablet ---------------------------------------------------- 2 to 10 lbs. 2.3 mg 46 mg 11 - 25 lbs. 5.75 mg 115 mg 26 - 50 lbs. 11.5 mg 230 mg 51 - 100 lbs. 23.0 mg 460 mg ---------------------------------------------------- Dogs over 100 lbs. are provided the appropriate combination of tablets.
The effectiveness of SENTINEL Tablets is based upon existing Novartis product approvals for milbemycin oxime (Interceptor Tablets, NADA 140-915) and lufenuron (Program Tablets, NADA 141-035).V. TAREGET ANIMAL SAFETYInterceptor Tablets containing milbemycin oxime are approved for the prevention of heartworm disease caused by Dirofilaria immitis, the control of adult Ancylostoma caninum (hookworm), and the removal and control of adult Toxocara canis, Toxascaris leonina (roundworm) and Trichuris vulpis (whipworm) infections in dogs. Program Tablets containing lufenuron are approved for use in dogs, for the prevention and control of flea populations.
Well-controlled studies demonstrated that SENTINEL was equivalent to Interceptor Tablets and Program Tablets against the labeled parasites. The SENTINEL dosage, route of administration (oral), active ingredients and claims are identical to those approved for Interceptor and Program.
A. Nematode Efficacy Studies
Thirteen studies were conducted in dogs to demonstrate the efficacy of milbemycin oxime against nematodes. See the Interceptor tablet Freedom of Information (FOI) summaries for more information (NADA 140-915).
B. Flea Efficacy Studies
Four efficacy studies were conducted in dogs to demonstrate the efficacy of lufenuron against fleas. See the Program tablet FOI summary for more information (NADA 141-035).
C. Component Efficacy Studies - SENTINEL Tablets
Five studies were conducted to confirm the dose and demonstrate component efficacy for both milbemycin oxime and lufenuron in a combination tablet. One study each was conducted to confirm efficacy against heartworm (Dirofilaria immitis), fleas (C. felis), roundworm (Toxocara canis), hookworm (Ancylostoma caninum), and whipworm (Trichuris vulpis). All studies were conducted in a double-blind manner using the proposed final market formulation.
1) Heartworm Efficacy Study
Purpose: SENTINEL tablets, Interceptor tablets and Program tablets were compared for efficacy against heartworms (Dirofilaria immitis).
Investigator: Byron Blagburn, Ph.D.
Study Location:
Auburn UniversityType of Study: Experimental infection with L3 larvae of Dirofilaria immitis.
Auburn, AlabamaAnimals: Forty Beagle dogs (20 males, 20 females, 1-4 years old) were divided into four groups of ten dogs each.
Dosage Forms: Group 1: Placebo Tablets
Group 2: Program (lufenuron) Tablets
Group 3: Interceptor (milbemycin oxime) Tablets
Group 4: SENTINEL (milbemycin oxime/lufenuron) TabletsRoute of Administration: Oral
Dose Tested: Milbemycin Oxime 0.5 mg/kg
Lufenuron 10 mg/kgFrequency of Treatment: One dose at 1, 2, 3, 4 and 5 months after infection.
Controls: Placebo control (group 1)
Duration of Study: Dogs experimentally infected with L3 larvae of Dirofilaria immitis. All dogs were euthanized and adult heartworms were counted six months post infection.
Results: Efficacy was calculated by comparing the number of adult heartworms in each of the treatment groups to the number of adult heartworms found in the control group. The following table shows the percent efficacy for each treatment group.
Treatment Geometric Mean % Efficacy ----------------------------------------------------------------- Placebo 1.39 ± 1.28 --- Lufenuron 1.40 ± .102 - 0.72% Milbemycin Oxime 0.0 ± 0.0 100% Combination 0.0 ± 0.0 100% -----------------------------------------------------------------No worms were recovered from the group which received milbemycin oxime, or the milbemycin oxime/lufenuron combination tablet; this represents 100% prevention of D. immitis.Conclusions: SENTINEL was better than the placebo and the lufenuron treatment groups. SENTINEL was similar to the milbemycin treatment group, indicating that lufenuron did not interfere with the activity of milbemycin when administered in combination.
Adverse Reactions: None reported.
2) Flea Efficacy Study
Purpose: SENTINEL tablets, Interceptor tablets and Program tablets were compared for efficacy against fleas.
Investigator: Byron Blagburn, Ph.D.
Study Location:
Auburn UniversityType of Study: Periodic infestation with newly emerged fleas throughout the study.
Auburn, AlabamaAnimals: Forty Beagle dogs (20 males, 20 females, 4-5 years old) were divided into four groups of ten dogs each.
Dosage Forms: Group 1: Placebo Tablets
Group 2: Program (lufenuron) Tablets
Group 3: Interceptor (milbemycin oxime) Tablets
Group 4: SENTINEL (milbemycin oxime/lufenuron) TabletsRoute of Administration: Oral
Dose Tested: Milbemycin Oxime 0.5 mg/kg
Lufenuron 10 mg/kgFrequency of Treatment: One treatment on day 16 or 17 of the study.
Controls: Placebo control (group 1)
Duration of Study: All dogs were infested with newly emerged adult fleas 2-3 times per week for 7 weeks and flea eggs were collected once weekly, placed in flea rearing medium and allowed to emerge.
Results: Efficacy was calculated by comparing the development of eggs collected from fleas feeding on each of the three treated groups versus control animals. The following table shows the cumulative developmental success rates between days 7 and 33 post-treatment (efficacy was based on the first month only based on the monthly dosing interval).
Treatment Group No. Fleas/No.Eggs Emergence Rate Collected ------------------------------------------------------------ Placebo 1535 / 2500 61.4% Lufenuron 178 / 2357 7.6% Milbemycin 1328 / 2220 59.8% Milbemycin/Lufenuron 171 / 2418 7.1% ------------------------------------------------------------Lufenuron tablets and milbemycin oxime/lufenuron combination tablets reduced flea emergence by 88.1 and 87.8%, respectively.Because fleas were recovered from dogs in each treatment group, treatment comparisons were made using logistic regression techniques and assuming a model containing treatment effects only. The Wald X2 test statistic was used to test for treatment differences using pairwise comparisons of treatment groups.
Treatment Comparisons Prob. >x2 ----------------------------------------------------------- Milbemycin/Lufenuron vs Placebo .0001 Milbemycin/Lufenuron vs Lufenuron .5241 Milbemycin/Lufenuron vs. Milbemycin .0001 ----------------------------------------------------------- Conclusions: SENTINEL was better than the placebo (p = .0001) and the milbemycin (p = .0001) treatment groups. The combination was similar to the lufenuron treatment group (p = .5241) indicating that milbemycin did not interfere with the activity of lufenuron when administered in combination.Adverse Reactions: None reported.
3) Roundworm Efficacy Study
Purpose: SENTINEL tablets, Interceptor tablets and Program tablets were compared for efficacy against roundworms (Toxocara canis).
Investigator: Dwight Bowman, Ph.D.
Study Location: CHK - R&D
Stanwood, MichiganType of Study: Natural infections of roundworms (Toxocara canis).
Animals: Forty adult dogs (22 male, 18 female) of various breeds were divided into four groups of ten dogs each.
Dosage Forms: Group 1: Placebo Tablets
Group 2: Program (lufenuron) Tablets
Group 3: Interceptor (milbemycin oxime) Tablets
Group 4: SENTINEL (milbemycin oxime/lufenuron) TabletsRoute of Administration: Oral
Dose Tested: Milbemycin Oxime 0.5 mg/kg
Lufenuron 10 mg/kgFrequency of Treatment: One treatment.
Controls: Placebo control (group 1)
Duration of Study: The dogs were euthanized 7 days after treatment and adult worms were recovered, identified and counted.
Results: Efficacy was calculated by comparing the number of worms collected from each of the treatment groups versus control animals. The following table shows the percent efficacy for each group.
Treatment Geometric Mean % Efficacy ----------------------------------------------------------------- Placebo 1.098 ± .510 --- Lufenuron .816 ± .508 25.7% Milbemycin Oxime .030 ± .095 97.3% Combination .060 ± .127 94.5% -----------------------------------------------------------------
Because worms were recovered from dogs in each treatment group, counts were logarithmically transformed and analysis of variance was done for the treatment comparisons of interest.Treatment Comparisons Two-sides p-values ---------------------------------------------------------- Milbemycin/Lufenuron vs Placebo .0001 Milbemycin/Lufenuron vs Lufenuron .0001 Milbemycin/Lufenuron vs. Milbemycin .8561 ----------------------------------------------------------Conclusions: SENTINEL was better than the placebo (p = .0001) and the lufenuron (p = .0001) treatment groups. The combination was similar to the milbemycin treatment group (p = .8561), indicating that lufenuron did not interfere with the activity of milbemycin when administered in combination.Adverse Reactions: None reported.
4) Hookworm Efficacy Study
Purpose: SENTINEL tablets, Interceptor tablets and Program tablets were compared for efficacy against hookworms (Ancylostoma caninum).
Investigator: Dwight Bowman, Ph.D.
Study Location:
CHK - R&DType of Study: Natural infections of hookworms (Ancylostoma caninum).
Stanwood, MichiganAnimals: Forty adult dogs (20 males, 20 females) of various breeds were divided into four groups of ten dogs each.
Dosage Forms: Group 1: Placebo Tablets
Group 2: Program (lufenuron) Tablets
Group 3: Interceptor (milbemycin oxime) Tablets
Group 4: SENTINEL (milbemycin oxime/lufenuron) TabletsRoute of Administration: Oral
Dose Tested: Milbemycin Oxime 0.5 mg/kg
Lufenuron 10 mg/kgFrequency of Treatment: One treatment.
Controls: Placebo control (group 1)
Duration of Study: The dogs were euthanized 7 days after treatment and adult worms were recovered, identified and counted.
Results: Efficacy was calculated by comparing the number of worms recovered from each of the three treatment groups versus control animals. The following table shows the percent removal for each group.
Treatment Geometric Mean % Efficacy ---------------------------------------------------- Placebo 1.426 ± .619 --- Lufenuron 1.099 ± .523 22.9% Milbemycin Oxime 0.030 ± .095 97.9% Combination .301 ± .763 78.9%* ---------------------------------------------------- * One dog harbored 253 worms at necropsy. A total of 3 worms were recovered from the remaining 9 dogs in this group.Because worms were recovered from dogs in each treatment group, counts were logarithmically transformed and analysis of variance was done for the comparisons of interest.
Treatment Comparisons Two-sided p-values ------------------------------------------------------- Milbemycin/Lufenuron vs Placebo .0001 Milbemycin/Lufenuron vs Lufenuron .0029 Milbemycin/Lufenuron vs. Milbemycin .2862 -------------------------------------------------------Conclusions: SENTINEL was better than the placebo (p = .0001) and was better than the lufenuron (p = .0029) treatment groups. The combination was similar to the milbemycin treatment group (p = .2862), indicating that lufenuron did not interfere with the activity of milbemycin when administered in combination.Adverse Reactions: None reported.
5) Whipworm Efficacy Study
Purpose: SENTINEL tablets, Interceptor tablets and Program tablets were compared for efficacy against whipworms (Trichuris vulpis).
Investigator: Dwight Bowman, Ph.D.
Study Location:
CHK - R&DType of Study: Natural infections of whipworms (Trichuris vulpis).
Stanwood, MichiganAnimals: Forty adult dogs (18 males, 22 females) were divided into four groups of ten dogs each.
Dosage Forms: Group 1: Placebo Tablets
Group 2: Program (lufenuron) Tablets
Group 3: Interceptor (milbemycin oxime) Tablets
Group 4: SENTINEL (milbemycin oxime/lufenuron) TabletsRoute of Administration: Oral
Dose Tested: Milbemycin Oxime 0.5 mg/kg
Lufenuron 10 mg/kgFrequency of Treatment: One treatment.
Controls: Placebo control (group 1)
Duration of Study: The dogs were euthanized 7 days after treatment and adult worms were recovered, identified and counted.
Results: Efficacy was calculated by comparing the number of worms recovered from each of the three treatment groups versus control animals. The following table shows the percent removal for each group.
Treatment Geometric Mean % Efficacy ---------------------------------------------------- Placebo 1.905 ± .701 --- Lufenuron 1.831 ± .678 3.9% Milbemycin Oxime .770 ± 1.36 59.6%* Combination .182 ± .345 90.4% ---------------------------------------------------- * One dog harbored 247 worms at necropsy. A total of 7 worms were recovered from the remaining 9 dogs in the group.Because worms were recovered from dogs in each treatment group, counts were logarithmically transformed and analysis of variance was done for the comparisons of interest.
Treatment Comparisons Two-sides p-values ---------------------------------------------------------- Milbemycin/Lufenuron vs Placebo .0001 Milbemycin/Lufenuron vs Lufenuron .0001 Milbemycin/Lufenuron vs. Milbemycin .5178 ----------------------------------------------------------Conclusions: SENTINEL was better than the placebo (p = .0001) and was better than the lufenuron (p = .0001) treatment groups. The combination was similar to the milbemycin treatment group (p = .5178), indicating that lufenuron did not interfere with the activity of milbemycin when administered in combination.Adverse Reactions: None reported.
D. Clinical Trials - SENTINEL Tablets
Two clinical field trials were conducted to supplement data obtained in the original clinical trials conducted under NADA 140-915 and NADA 141-035. The General Clinical Trial demonstrated efficacy against four target parasites; fleas, roundworms, hookworms and whipworms. The Roundworm Clinical Trial generated additional information on roundworm efficacy.
1) General Clinical Trial
Purpose: To evaluate SENTINEL tablets in clinical use.
Investigators/Study Locations:
Mildred Bass, DVM Mark Epstein, DVM (Site 3) Jim Raab, DVM Village Veterinary Clinic Paw Creek Animal Hospital Tri-County Animal 12249 Kingston Pike 11226 Mount Holly Road Hospital Farragut, TN 37922 Charlotte, NC 28214 1807 Okeechobee Road Fort Pierce, FL 34950 Alan Bater, MRCVS Mark Epstein, DVM (Site 4) Denis Scarpinato, DVM Freeport Animal Clinic Bethel Animal Hospital Pinewoods Animal P.O. Box F-724 125 Forest Oaks Drive Hospital Freeport, Grand Bahamas Lake Wylie, SC 29710 1905 43rd Vero Beach, FL 32960 Gary Brotze, DVM Jerry Greene, DVM Scott Siegel, DVM Creekview Veterinary Clinic Academe Animal Hospital Logan Animal Hospital 1121 Eikel 912 East Fletcher Avenue 103 Justice Avenue New Braunfels, TX 78130 Tampa, FL 33612 Logan, WV 25601 Jay Butan, DVM Joe Kinnarney, DVM Jan Strother, DVM Canal Animal Hospital Reidsville Veterinary No. Alabama Cat & 501 24th Avenue, North Hospital Bird Veterinary Clinic Lake Worth, FL 33460 1401 West Harrison St. Route 4, Box 92 Reidsville, NC 27320 Hartselle, AL 35640 Bill Campaigne, DVM John Lewis, DVM Gary Wilson, DVM Seguin Animal Hospital Madison Veterinary Clinic Animal Hospital of 1252 West Kingsbury 1309 West Base St. New Caney Seguin, TX 78155 Madison, FL 32340 Route 2, Box 1060 New Caney, TX 77357 Mark Epstein, DVM (Site 1) Ann Parker, DVM Karen Wylie, DVM Forestbrook Animal Hope Mills Road Animal Leland Animal Clinic Hospital Hospital 302 Bankhead 3200 Union Road 2301 Hope Mills Road Highway Gastonia, NC 38056 Fayetteville, NC 28304 Mableton, GA 30059 Mark Epstein, DVM (Site 2) New Hope Animal Hospital 3435 South New Hope Rd. Gastonia, NC 28056Type of Study: Natural infections (fleas, roundworms, hookworms and whipworms) in pet dogs.Animals: Two hundred sixty-nine (269) client owned dogs were enrolled in the study and two hundred forty-seven (247) were included in the final efficacy analysis.
Dosage Form: SENTINEL (Milbemycin Oxime/Lufenuron) Tablets
Route of Administration: Oral
Dose Tested: Milbemycin Oxime 0.5 mg/kg
Lufenuron 10 mg/kgFrequency of Treatment: Six monthly doses.
Controls: None
Duration of Study: Each dog was dosed monthly with the test drug for six months. Each dog was evaluated every month by the clinical investigator. Flea counts were performed every month. Testing for heartworms by occult testing and microfilariae examination was done on all dogs over 6 months of age; at enrollment, at month three and at month six of the study. Fecal flotation for gastrointestinal parasites was performed at enrollment, at month 1, 2 and 3 and at follow-up examinations 7-18 days after any positive fecal.
Results: Efficacy was evaluated against roundworm, hookworm, and whipworm after 3 months. Efficacy against fleas was evaluated after 6 months of administration. The results are displayed in the following table.
Parasite Treatment/Reduction Control % (number % (number of dogs) of dogs) ------------------------------------------------------------------------- Roundworm 96.5% (57) 100.0% (38) Hookworm --- 87.3% (103) Whipworm 89.3% (56) 93.0% (43) Flea Count Reduction1 82.5% (161) --- Dogs With Adequate Flea Control2 -- 85.7% (161) ------------------------------------------------------------------------- 1- Flea reduction evaluated in dogs kept in controlled environments only; i.e., dogs that had frequent contact with untreated animals and/or untreated environments were excluded from analysis. 2- The majority (> or = 82%) of dogs showed adequate control of flea populations with flea counts of five or fewer at months four, five and six. Due to the length of the trial (6 months) and the prepatent period of the heartworm (approximately 6.5 months), the efficacy of the drug for the prevention of heartworms could not be scientifically evaluated.Conclusions: SENTINEL tablets provided adequate efficacy against the target parasites.
Adverse Reactions: The following clinical observations were noted during the 6 month study.
Observation Number of Percent of Dogs Dogs n = 269 --------------------------------------------------- Diarrhea 8 3.0% Vomiting 6 2.2% Anorexia 4 1.5% ---------------------------------------------------2) Roundworm Clinical TrialPurpose: To evaluate SENTINEL tablets in clinical use against roundworms.
Investigators/Study Locations:
Mildred Bass, DVM Denis Scarpinato, DVM Gary Wilson, DVM Village Veterinary Clinic Pinewoods Animal Animal Hospital of New 12249 Kingston Pike Hospital Caney Farragut, TN 37922 1905 43rd Route 2, Box 1060 Vero Beach, FL 32960 New Caney, TX 77357 Alan Bater, MRCVS Scott Siegel, DVM Karen Wylie, DVM Freeport Animal Clinic Logan Animal Hospital Leland Animal Clinic P.O. Box F-724 103 Justice Avenue 302 Bankhead Highway Freeport, Grand Bahamas Logan, WV 25601 Mableton, GA 30059 Ann Parker, DVM Hope Mills Road Animal Hospital 2307 Hope Mills Road Fayetteville, NC 28304Type of Study: Natural infections by roundworms in pet dogs.Animals: Fifty seven (57) client owned dogs were enrolled in the study. Thirty-eight (38) were placed in the SENTINEL treatment group and nineteen (19) placed in the pyrantel pamoate group.
Dosage Form: SENTINEL (Milbemycin Oxime/Lufenuron) Tablets
Pyrantel PamoateRoute of Administration: Oral
Dose Tested: SENTINEL ( Milbemycin Oxime 0.5 mg/kg/Lufenuron 10 mg/kg)
Pyrantel Pamoate (labeled dose)Frequency of Treatment: One or two monthly doses.
Controls: Pyrantel Pamoate
Duration of Study: Each dog had roundworms at the start of the trial, and was given the test drug or pyrantel pamoate. A fecal examination was performed 7-18 days later. The dogs returned one month after the first dose and were checked again for roundworms. If positive, they were dosed again and checked 7-18 days later, if negative, they were finished at the month one examination. All remaining dogs were finished at the month one follow-up fecal.
Results: Efficacy was evaluated against roundworms and is displayed in the following table.
Test Article Removal Claim Control Claim --------------------------------------------------- Combination 97.5% 85.7% Pyrantel pamoate 76.5% 84.6% ---------------------------------------------------Conclusions: Based on an odds ratio test, SENTINEL was no worse than the positive control in the removal and control of roundworms.Adverse Reactions: The following clinical observations were noted during study.
Number and Percent of Dogs ------------------------------ Observation Combination Pryantel Pamoate (n = 38) (n = 19) ------------------------------------------------ Diarrhea 1 (2.6%) 1 (5.3%) Vomiting 3 (7.9%) 0 (0.0%) ------------------------------------------------
A. Milbemycin Oxime Safety StudiesVI. HUMAN SAFETYSix target animal safety studies were conducted in dogs to address the safety of milbemycin oxime. See the Interceptor Tablet FOI Summaries for more information.
B. Lufenuron Safety Studies
Nine target animal safety studies were conducted in dogs to address the safety of lufenuron. See the Program Tablet FOI Summary for more information.
C. SENTINEL Safety Studies
Three target animal safety studies were conducted in dogs to address the safety of the milbemycin oxime/lufenuron combination drug.
1) Acute Oral Toxicity Study in Dogs with Milbemycin Oxime/Lufenuron Combination Tablet
Purpose: To evaluate the safety of SENTINEL (milbemycin oxime/lufenuron) tablets when given at 10X the projected use rate.
Investigator: Dennis J. Naas, BS
Study Location:
Wil Research LaboratoriesType of Study: Laboratory safety study
Ashland, Ohio
Animals: Twelve Beagle dogs (6 males, 6 females, 15-24 months of age)Dosage Forms: Group 1: Placebo Tablets (vehicle)
Group 2: SENTINEL TabletsRoute of Administration: Oral
Dose Tested: Milbemycin Oxime 5.0 mg/kg (10X the monthly use rate)
Lufenuron 100 mg/kg (10X the monthly use rate)Frequency of Treatment: One dose.
Controls: Group 1: Placebo control group.
Duration of Study: The animals were observed twice daily for signs of mortality and morbidity. The animals were also observed for clinical signs at the time of dosing and at 1, 2, 4, 8, 12 and 24 hours following dosing. Animals were also observed daily for a two-week observation period following dosing.
Veterinary examinations were conducted prior to the initiation of dosing and prior to necropsy. Individual body weights were recorded weekly. Food consumption was recorded daily and reported weekly. Clinical pathology evaluations (hematology, serum chemistry and urinalysis) were performed on week -1 (pretest), 0 and 2. Complete necropsies were performed on each dog.
Results: All animals survived to the scheduled necropsy. The following clinical observations were recorded during the study: vomiting-- 3 dogs in the placebo group at 4, 11, and 13 days post treatment and 4 dogs in the combination group at 1, (2 and 12)*, 4 and 12 days post treatment; salivation--1 dog in the combination group at 0, 1 and 2 hours post treatment.
*one dog vomited twice, at day 2 and day 12.
Mean body weights, body weight changes and food consumption were unaffected by treatment. No clinically significant changes were apparent in the hematology, serum chemistry and urinalysis parameters. Macroscopic findings were unaffected by treatment.
Conclusions: Milbemycin oxime/lufenuron combination tablets are safe when administered orally to beagle dogs at dose levels of 5 mg/kg milbemycin oxime and 100 mg/kg lufenuron (10X the month ad usum level). Vomiting was observed in 3 placebo (vehicle)-treated dogs and in 4 combination-treated dogs. Salivation was noted in 1 dog treated with the combination drug for up to 2 hours post treatment.
2) A 2-Month Oral Toxicity Study of Milbemycin Oxime/Lufenuron Tablets in Beagle Puppies, Starting at Two Weeks of Age
Purpose: To evaluate the safety of SENTINEL (milbemycin oxime/lufenuron) tablets when given at up to 5X the projected use rate to puppies.
Investigator: Dennis J. Naas, BS
Study Location:
Wil Research LaboratoriesType of Study: Laboratory safety study
Ashland, OhioAnimals: Forty-eight (24 males, 24 females) 2-week old Beagle puppies were divided into four groups of six males and six females. The puppies remained with the lactating bitches until weaning was completed.
Dosage Forms: Group 1: Placebo Tablets (vehicle)
Group 2: SENTINEL (milbemycin oxime/lufenuron) Tablets at 1X
Group 3: SENTINEL (milbemycin oxime/lufenuron) Tablets at 3X
Group 4: SENTINEL (milbemycin oxime/lufenuron) Tablets at 5XRoute of Administration: Oral
Dose Tested: 1X - Milbemycin Oxime 0.5 mg/kg
Lufenuron 10 mg/kg
3X - Milbemycin Oxime 1.5 mg/kg
Lufenuron 30 mg/kg
5X - Milbemycin Oxime 2.5 mg/kg
Lufenuron 50 mg/kgFrequency of Treatment: Single doses on days 0, 14, 28, 42 and 56.
Controls: Group 1: Placebo (vehicle) control group.
Duration of Study: All puppies were observed twice daily for signs of morbidity and mortality until one week after the last dose. Observations included clinical signs, (twice daily and hourly for 8 hours on the days of dosing), body weight (twice weekly), hematology, serum chemistry, ophthalmic exams (weeks 4 and 8), gross pathology and organ weights.
Results: Four deaths occurred (two females in the control, one male in the 1X and one male in the 5X groups); the deaths were not attributed to the test drug.
CNS/behavior findings occurred in the 3X and 5X groups early in the study period (when puppies were 2-4 weeks of age). These findings consisted predominantly of incoordination, generalized tremors and unable to be aroused. These clinical signs were limited to pups in the 5X dose group following the first and/or second dosing (study days 0 and 14, respectively) and pups in the 3X dose group following the first dose only. In some cases the CNS/behavior findings persisted for one or two days following test article administration. All affected animals showed full recovery. Tail twitching was observed for one male in the 5X group after the first dose, persisting for 3 days. None of the aforementioned signs were observed after the third, fourth and fifth dosings (study days 28, 42 and 56, respectively).
No adverse effects were observed on body weights, body weight gains or hematology and serum chemistry parameters. No adverse effects were observed at the ophthalmic and macroscopic examinations. Organ weights were unaffected by treatment.
Conclusions: SENTINEL caused changes in CNS/behavior (incoordination, generalized tremors, inability to arouse and/or tail twitching) in 2-week-old puppies treated at 3X and 5X the recommended dose and in 4-week-old puppies treated at 5X the recommended dose.
3) A 6-Month Oral Toxicity Study of Milbemycin Oxime/Lufenuron Tablets (SENTINEL) in Young Beagle Dogs
Purpose: To evaluate the safety of SENTINEL (milbemycin oxime/lufenuron) tablets when given at doses up to 5X the projected use rate to dogs for six months.
Investigator: Dennis J. Naas, BS
Study Location:
Wil Research LaboratoriesType of Study: Laboratory safety study
Ashland, OhioAnimals: Forty-eight (24 males, 24 females) 2 month old Beagle puppies were divided into four groups of six males and six females.
Dosage Forms: Group 1: Placebo Tablets
Group 2: SENTINEL (milbemycin oxime/lufenuron) Tablets at 1X
Group 3: SENTINEL (milbemycin oxime/lufenuron) Tablets at 3X
Group 4: SENTINEL (milbemycin oxime/lufenuron) Tablets at 5XRoute of Administration: Oral
Dose Tested: 1X - Milbemycin Oxime 0.5 mg/kg
Lufenuron 10 mg/kg
3X - Milbemycin Oxime 1.5 mg/kg
Lufenuron 30 mg/kg
5X - Milbemycin Oxime 2.5 mg/kg
Lufenuron 50 mg/kgFrequency of Treatment: Single doses per day for three sequential days starting on days 0, 28, 53, 87, 112, 140, 171 and 200.
Controls: Group 1: Placebo (vehicle) control group.
Duration of Study: All dogs were observed until 3 or 4 days after the last dose. Observations included clinical signs, body weight, food consumption, periodic hematology, serum chemistry, urinalysis, ophthalmic examinations as well as gross pathology, organ weight and histopathology.
Results: All animals survived to the scheduled necropsy at week 29. The following clinical observations are considered probably related to treatment with either the active combination tablet or the vehicle control tablet: Diarrhea/soft stools, vomiting, and red, raised skin lesions. Salivation was noted in 7 dogs (2 at 1X, 2 at 3X and 3 at 5X). Six of these 7 dogs salivated either at the time of dosing or within 1 hour after a treatment.
Mean body weight changes, food consumption and organ weights were unaffected by treatment. No abnormal changes were apparent when hematology, serum chemistry and urinalysis parameters were evaluated. Ophthalmic examinations revealed no adverse findings.
Conclusions: SENTINEL is safe for use in dogs and puppies 2 months of age and older at doses up to 5X the recommended dose.
Data on human safety, pertaining to consumption of drug residues in food, were not required for approval of this NADA. This drug is to be labeled for use in dogs which are non-food animals.VII. AGENCY CONCLUSIONS
The data in support of this NADA comply with the requirements of Section 512 of the Act and Section 514 of the Implementing regulations. The data demonstrate that SENTINEL Tablets (milbemycin oxime/lufenuron), when used under labeled conditions of use are safe and effective.8. Labeling (Attached)The drug is restricted to use by or on the order of a licensed veterinarian because professional expertise is judged to be critical for the diagnosis of heartworms, whipworms and hookworms and for the safe use of the product.
Under section 512(c)(2)(F)(ii) of the Federal Food, Drug and Cosmetic Act, this approval for non food producing animals qualifies for THREE years of marketing exclusivity beginning on the date of approval because the application contains substantial evidence of the effectiveness of the drug involved and studies of animal safety required for the approval of the application and conducted or sponsored by the applicant.
A. Package Inserts
1. Veterinarian's Insert
2. Client's Insert
B. Blister Cards (6 Tablets)
C. Bulk Package (60 Tablets)
D. Dispensing Envelope
Outer Flap
Inner Flap
Front
Back
Copies of applicable labels may be obtained by writing to the:
Freedom of Information Office
Center for Veterinary Medicine, FDA
7500 Standish Place
Rockville, MD 20855