Equivalence Among Antiepileptic Drug Generic and Brand Products in People With Epilepsy: Single-Dose 6-Period Replicate Design (EQUIGEN Single-Dose Study)

The study proposed in this protocol will determine if bioequivalence testing performed for
the FDA translates into similar bioequivalence in a population of people with epilepsy when
switching among different generics of the anti-epileptic drug (AED). Based on a variety of
pharmacokinetic (PK) data and clinical reports of concern, the example anti epilepsy drug
(AED) used for this study will be lamotrigine (LTG).

In this single dose study, people with epilepsy taking AEDs, but not currently taking the
test medication, lamotrigine, will be studied. We will use an order-randomized three-sequence
six-period replicate design with the two most disparate generics studied in two replicate
periods each and the brand (reference) product studied in two additional periods. A standard
single dose of the test drug (lamotrigine 25mg) will be administered under controlled
conditions (fasting with subsequent standardized meals) with a 12-hour in-facility blood
sample collection followed by a collection every 24 hours for a total of a 96 hour sample
collection that will be used to establish the pharmacokinetic measures of Cmax, AUC96 and
AUC∞. Each period will be separated by at least a 12 day washout interval.

The replicate studies will be used to determine the intra-individual variability of the
pharmacokinetic responses of the brand and the two generic products, as well as
subject-by-formulation interaction variances. The data will also be used to calculate
simultaneously all parameters that are needed to compare the 3 products in average and
individual bioequivalence and outlier analyses. The differences between the disparate
generics will be used to establish if the current standards translate to equivalence within
the limits of the brand intra-subject variation.

The factors we will use to determine the most disparate generics include the results from the
in vivo data from the ABE studies submitted to the FDA in the ANDA and in vitro chemical
assay (potency) and dissolution data performed on several currently available lots. The
intent is to study the specific lot of the generic product predicted to result in the lowest
levels and compare it to the specific lot from another generic product predicted to result in
the highest levels. Similarly, if multiple lots of the brand products are available, we will
perform in vitro testing to establish the most desirable lot to study.

Factors that alter metabolism, including concomitant AEDs that may have hepatic enzyme
induction effects will be tracked but not excluded, as long as the dose remains constant, as
the goal is to reproduce the 'real life' situation as closely as possible within the
practical limits of funding and study size. Subjects receiving valproate as concomitant
medication will be excluded because the prolongation of half life would not allow LTG to
reliably be completely cleared by 13 days. The criteria that establish an enriched population
will also be tracked and used in a secondary analysis, but will not be used as an inclusion
requirement. The enriched population is defined as people who experienced an otherwise
unexplained increase in seizures or adverse effects, or a substantial change in AED level
after a switch in AED products.

The discovery of any subject-by-formulation interaction outliers (i.e. subjects with
differential pharmacokinetic reactions to a pair of formulations) will raise considerable
concerns about equivalence. Recently established methods in the statistical analysis of
outliers in crossover studies will be used to determine if any outliers are present.

Qualified subjects will be screened and upon fulfilling inclusion/exclusion criteria and
signing the informed consent will be enrolled in the study and enter the randomization phase
(2-30 days). Subjects will be randomized according to a sealed allocation list that will be
balanced for sequence and provided to each site prior to the first subject enrollment.
Subjects that withdraw prior to completing the third period will be replaced in a randomized
manner. The randomization list will be generated by the study statistical group. There are
six test periods in three sequences for a sequence-randomized study. During two test periods
subjects will receive a single dose of the brand AED and during the other four test periods
subjects will receive a single dose from one of the two investigated generics (each twice).
The single doses will be administered in the fasting state during an in-facility 12-hour
pharmacokinetic session to collect samples to determine Cmax and AUCs. Four additional
samples will be drawn at 24, 48, 72, and 96 hours after the dose as an outpatient (making
each pharmacokinetic test last for 4 days). Each in-facility pharmacokinetic testing will be
separated by a 12-23 day washout period; consistent washout periods of 14 days will be
preferred. A final follow-up phone evaluation will be conducted 12-16 days (target 14 days)
after the last dose. During the study the subjects will continue their usual concomitant
medications, including AEDs, without change.

Investigators will compare the AED levels as measured by Cmax and AUC in each group using
average bioequivalence (ABE) and individual bioequivalence (IBE) criteria. Average
bioequivalence will be established if the 90% confidence intervals of the geometric mean of
Cmax and AUCs for the most disparate generic products compared to each other are entirely
within the 80%-125% range (the FDA criteria for bioequivalence) using the two one-sided
standard analyses. Otherwise the products will be considered to not be bioequivalent.
Similarly, the products will be considered to not be bioequivalent if the criteria for IBE
for each generic product compared to the brand product are not met.

Study Population: Approximately 54 subjects (45 subjects to completion).

Number of centers: 3 sites enrolling approximately 18 subjects each.

Duration of study: Approximately 1 year.

Inclusion Criteria

Eligible subjects must satisfy the criteria below at the time of enrollment:

1. 18 years or older.

2. BMI not less than 18.5 and weight not less than 110 pounds.

3. Not donated blood within the past 56 days before the first pharmacokinetic testing.

4. Agrees not to donate blood at any time during the trial and for 56 days after the
final PK in-facility admission.

5. Has epilepsy for at least one year based on site PIs assessment.

6. Taking at least one AED, which is not the study medication (lamotrigine).

7. No changes in AED regimen for at least 28 days prior to first pharmacokinetic testing.

8. Have the ability to understand the informed consent form and be willing to provide
informed consent.

9. Willing to remain on same AED regimen through entire study. Subjects will be
responsible to supply all of their concomitant medications (except for the study
medication, lamotrigine).

10. Willing to stay approximately 14 hours in the research facility on six separate
occasions for pharmacokinetic testing.

11. Willing to fast overnight and the morning of each of the six pharmacokinetic testing
sessions.

12. Willing to have at least 23 blood samples collected during the pharmacokinetic testing
including the in-facility session and each of the following four mornings for 96 hours
post the study medication dose to complete the sample collection for each of the 6
periods. The in-facility blood collections will mainly be performed using an inserted
catheter. In the event of difficulty with the catheter, samples may be drawn by
venipuncture. The outpatient collections will be drawn by venipuncture. The total
amount of blood during each PK session will be equal to about 14 teaspoons (66.5
milliliters). The total amount of blood drawn throughout the entire study will be
about 96 teaspoons (478.5 milliliters) or less. For reference, this amount is
approximately equal to the quantity of blood drawn during a standard blood donation by
the Red Cross.

13. Willing to completely abstain from alcohol consumption for at least 24 hours prior to
each pharmacokinetic testing admission until after the last sample is drawn for each
period (~96 hours after the initial dose at each pharmacokinetic admission). We
encourage no or minimal alcohol use throughout the study, but alcohol is not
restricted at other times.

14. Willing to remain on a consistent regimen of concomitant medications including
over-the-counter drugs and herbal drugs, if they are being used and deemed to possibly
affect the metabolism of the study medication.

15. Willing to not eat grapefruit or drink grapefruit juice through the duration of the
study.

16. If a tobacco user, willing to continue with the same pattern of tobacco use, except
that no tobacco use is permitted during the PK facility admissions of approximately 14
hours (includes all tobacco products).

17. Willing to complete the subject diary as outlined in the protocol.

18. Willing to adhere to all other protocol requirements as outlined in the informed
consent document.

19. Females must be either of non-childbearing potential (defined as having undergone
surgical sterilization or postmenopausal (greater than 50 years old and amenorrhea for
greater than or equal to 12 months) or must be using at least one acceptable method of
contraception as follows:

1. Double-barrier method (e.g. condom plus spermicide, condom plus diaphragm with
spermicide)

2. Hormonal contraceptive treatment (progesterone only agents - use of any agents
containing estrogen are an exclusion for the lamotrigine testing)

3. Intrauterine Device (IUD)

4. Monogamous relationship with a vasectomized partner

5. Abstinent for 8 weeks prior to and throughout the study.

20. Subject must be at least 28 days from last participation in any other study.

Exclusion Criteria

1. Progressive CNS disorder that could influence adverse effects or seizure control.

2. Known medication non-adherence. Non-adherence is assessed by the investigator based on
the procedures defined in the manual of procedures.

3. Taking the study medication (lamotrigine) within 28 days of enrollment.

4. Use of valproate (as divalproex sodium or valproic acid), any form of estrogens,
rifampin, orlistat, felbamate or sertraline within 28 days of study entry.

5. Subject has a history of alcohol or substance abuse within 1 year prior to screening
for study participation, or is currently using alcohol, drugs of abuse, or any
prescribed or over-the-counter medication in a manner, which, in the opinion of the
Investigator, indicates abuse.

6. History of psychogenic seizures within the past 2 years.

7. Any clinically significant psychiatric illness or psychological or behavioral problem
which, in the opinion of the investigator, could interfere with the subject being able
to participate in the study or comply with the study requirements. .

8. Any clinically significant laboratory abnormality or illness which, in the opinion of
the investigator, could interfere with the conducting or interpretation of the study
or put the subject at risk.

9. History of allergic reaction with past use of the study medication (lamotrigine).

10. More than two allergic reactions (actual allergy, not medication intolerance) to an
AED or one serious hypersensitivity reaction to an AED.

11. History of adverse effect associated with past use of the study medication
(lamotrigine) which, in the opinion of the investigator, could pose substantial risk
to the subject if it occurred during the trial.

12. Pregnant or lactating within 56 days of enrollment.

13. Unstable seizure control that makes AED changes likely during the course of the study.

14. Use of rescue AEDs (e.g. benzodiazepines) during more than two weeks of the 2 months
prior to enrollment.

15. Subject is in the process of quitting smoking within 28 days of study entry or plans
to quit smoking during the period of time the study will be conducted.