Dr. Dipa Brahmbhatt VMD MpH Ms DRUG DEVELOPMENT AND CONTROL Chapter 2 Dr. Dipa Brahmbhatt VMD MpH Ms

The development of drugs is both lengthy and expensive: * average of 7 years of testing * usually costs millions of dollars Many steps are involved (you’ll need time AND money)

DRUG DEVELOPMENT Stage 1) The ___________or synthesis of a new drug with the potential for therapeutic value __________________________ Series of tests run on computer models Testing in lab media,____________, or fungi to see if the drug produces the desired effect Observed side effects

STAGE 2 - If the results are satisfactory, – ______________________________________ – Drugs safety and effectiveness – Laboratory animals / _____________ species – Short-term and long-term tests – Check for immediate drug reactions, organ damage, reproductive effects, carcinogenicity, and _________________________ Submit _______________________ (INAD) application for the drug to the FDA – Clinical trials begin once application is approved DRUG DEVELOPMENT

Scientists are looking for signs of : - S hort-term toxicity: reactions occurring _______________ after dosing such as convulsions or paralysis - Long-term toxicity: ______________ months of regular dosing to check for organ damage. Animal is euthanized to examine the effects on tissues. - Systems-oriented screening: tests the drug’s effect on the body systems – specifics on how it affects the_____________________, nervous systems, etc. - Reproductive effects: does it effect ovulation, conception, or _____________________ -Carcinogenicity: do large doses for a prolonged time cause tumors? -Teratogenicity: are __________________ caused by administering the drug to pregnant animals?

Examples of teratogenicity

Stage 2 – If the preclinical trials are OK – Application for an INAD (Investigational New Animal Drug) is filed with the FDA – NOTE: Pesticide  EPA (Environmental Protection Agency), biologic (vaccines)  USDA – The FDA responds within ____________ days for approval DRUG DEVELOPMENT

Stage 2 – Phase I: Dose finding – Limited clinical trials – __________________ species – Drug safety and effectiveness – Short-term and long-term toxicity and effectiveness studies – Toxicity, SE, tissue residue, withdrawal time – _______________________________ – Pharmacokinetics DRUG DEVELOPMENT

Stage 2 – Phase II: Efficacy/Activity – Target species with ___________ or condition – Large scale clinical trials – Different locations – Submit ______________________________________ (NADA) to FDA (USDA/EPA) DRUG DEVELOPMENT

Stage III – Phase III: Comparative Target species Monitor drug efficacy and adverse reactions _____________________________ new drugs to existing treatments – Approval and license are granted for successful drugs

DRUG DEVELOPMENT Stage IV: Postmarketing surveillance stage – The drug company and the government monitor (active versus passive) the product as long as the drug is manufactured – This monitoring ensures product safety and efficacy

Figure 2-1

ADVERSE REACTIONS Pre-approval clinical trials Following treatment with REVOLUTION, transient localized alopecia with or without inflammation at or near the site of application was observed in approximately 1% of 691 treated cats. Other signs observed rarely (≤0.5% of 1743 treated cats and dogs) included vomiting, loose stool or diarrhea with or without blood, anorexia, lethargy, salivation, tachypnea, and muscle tremors. Post-approval experience In addition to the aforementioned clinical signs that were reported in pre- approval clinical trials, there have been reports of pruritis, urticaria, erythema, ataxia, fever, and rare reports of death. There have also been rare reports of seizures in dogs (see WARNINGS)

SAFETY REVOLUTION has been tested safe in over 100 different pure and mixed breeds of healthy dogs and over 15 different pure and mixed breeds of healthy cats, including pregnant and lactating females, breeding males and females, puppies six weeks of age and older, kittens eight weeks of age and older, and avermectin-sensitive collies. A kitten, estimated to be 5–6 weeks old (0.3 kg), died 8 1⁄2 hours after receiving a single treatment of REVOLUTION at the recommended dosage. The kitten displayed clinical signs which included muscle spasms, salivation and neurological signs. The kitten was a stray with an unknown history and was malnourished and underweight (see PRECAUTIONS).

Dogs In safety studies, REVOLUTION was administered at 1, 3, 5, and 10 times the recommended dose to six-week-old puppies, and no adverse reactions were observed. The safety of REVOLUTION administered orally also was tested in case of accidental oral ingestion. Oral administration of REVOLUTION at the recommended topical dose in 5- to 8-month-old beagles did not cause any adverse reactions. In a pre-clinical study selamectin was dosed orally to ivermectin-sensitive collies. Oral administration of 2.5, 10, and 15 mg/kg in this dose escalating study did not cause any adverse reactions; however, eight hours after receiving 5 mg/kg orally, one avermectin-sensitive collie became ataxic for several hours, but did not show any other adverse reactions after receiving subsequent doses of 10 and 15 mg/kg orally. In a topical safety study conducted with avermectin-sensitive collies at 1, 3 and 5 times the recommended dose of REVOLUTION, salivation was observed in all treatment groups, including the vehicle control. REVOLUTION also was administered at 3 times the recommended dose to heartworm infected dogs, and no adverse effects were observed. Cats In safety studies, REVOLUTION was applied at 1, 3, 5, and 10 times the recommended dose to six-week-old kittens. No adverse reactions were observed. The safety of REVOLUTION administered orally also was tested in case of accidental oral ingestion. Oral administration of the recommended topical dose of REVOLUTION to cats caused salivation and intermittent vomiting. REVOLUTION also was applied at 4 times the recommended dose to patent heartworm infected cats, and no adverse reactions were observed. In well-controlled clinical studies, REVOLUTION was used safely in animals receiving other frequently used veterinary products such as vaccines, anthelmintics, antiparasitics, antibiotics, steroids, collars, shampoos and dips.

Safety and Effectiveness Evaluation Short-term tests – hours following a test dose – check the animal for obvious _____________ reactions Long-term tests – typically run for 3 to 24 months of repeated dosing – check the animal’s various __________ systems for toxicity damage

Safety and Effectiveness Evaluation Special tests (Short/ Long term tests) – Reproductive affects Conception, fertilization, pregnancy – Carcinogenicity _________________ causing – Teratogenicity Fetal defects in pregnant animals

Toxicity Evaluation Conducted on mice ________________ dose that results in tissue and organ damage Highest dose that results in permanent injury or ________________

Effective and Lethal Dose Effective dose: the amount of the test drug (dose) that causes a __________________ in 50% of the animals that receive it – ED 50 _______________________ : the amount of the test drug that kills 50% of the animals that receive it – LD 50

LD 50

Therapeutic Index Therapeutic index is the drug dosage or dose that produces the__________________ with _________________ or no signs of toxicity – Also called the margin of safety – Determined by comparing the lethal dose and effective dose of the drug – LD 50 ÷ ED 50 – A wide therapeutic index means that the drug can produce its desired effect without approaching __________________

. Drug A is designed to lower heart rate (n=100) – It causes 50% of the mice to have a lower heart rate at a dosage of 2 mg/lb. – Effective dose: ED 50 = ________mg/lb – Drug A is then given at 100 mg/lb and 50% of the mice die – Lethal dose: LD 50 = ______________ mg/lb – TI = LD 50 /ED 50 = 100 mg/lb ÷ 2 mg/lb = ______ – Since the Therapeutic Index is 50, one would have to ingest ___________ times the effective dose to ingest the ______________ dose Therapeutic Index: Which Drug is Safer?

Drug B is also used to lower heart rate. It is given to 100 mice and produces a lower heart rate in 50 mice at 10 mg per pound (effective dose) When Drug B is given at a dose of 20 mg per pound, 50 mice die (lethal dose) TI = LD 50 /ED 50 = 20 mg per lb/10 mg per lb = 2 For Drug B, the TI is 2, which means that one would have to ingest _________________ the effective dose to ingest the lethal dose

Therapeutic Index: Which Drug is Safer? DRUG A: TI = 50 DRUG B: TI = 2 DRUG A has the higher ______________ INDEX or ___________________________________

Additional Testing Systems-oriented screening – After toxicity studies – Specific _______________________ / body system Evaluation of long-term effects (Chronic studies) – 3 months – 2 yrs – Histopathology Evaluation of reproductive effects, carcinogenicity, and teratogenicity

CHARLEY OVY an example of teratogenicity- cerebellar hypoplasia (most likely due to vaccination of the queen during gestation)

MEDICAL CALCULATION 2 How many mg of drug should be given to a patient who weighs 22 lbs. if the dosage is 0.2 mg/kg body weight? 50% dextrose = mg/ml?