Calf Deep Vein Thrombosis Treatment Trial

This is a randomized double-blind placebo controlled superiority clinical trial. Patients
will be identified at the time of the diagnosis of acute calf deep vein thrombosis and
approached at that time. If they agree they would be randomly assigned to placebo or apixaban
treatment for three months. Along with this they will also undergo repeat ultrasounds at 7,
14, and 90 days along with telephone follow-up at 30 and 60 days.

Inclusion Criteria

1. Age range: ≥ 18 years.

2. Both males and females

3. Confirmed acute calf vein thrombosis confined to either the deep (posterior tibial,
anterior tibial, or peroneal) or muscular (gastrocnemius or soleal) veins.

4. Negative serum or urine pregnancy test done (within 2 weeks) prior to randomization,
for women of childbearing potential only. Note: A woman of childbearing potential
(WOCBP) is defined as any female who has experienced menarche and who has not
undergone surgical sterilization (hysterectomy or bilateral oophorectomy) and is not
postmenopausal. Menopause is defined as 12 months of amenorrhea in a woman over age 45
years in the absence of other biological or physiological causes.

5. Ability to provide written informed consent.

Exclusion criteria

1. Any of the following because this study involves an investigational agent whose
genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are
unknown:

- Pregnant women

- Nursing women

- Men or women of childbearing potential who are unwilling to employ adequate
contraception Note: Women of child bearing potential must agree to follow
instructions for method(s) of contraception for the duration of treatment with
study drug(s) plus 33 days after finishing the last dose.

Males who are sexually active with WOCBP must agree to follow instructions for
method(s) of contraception for the duration of treatment with study drug(s) plus 93
days after finishing the last dose.

Azoospermic males and WOCBP who are continuously not heterosexually active are exempt
from contraceptive requirements. However they must still undergo pregnancy testing as
described in this section.

Note: Investigators shall counsel WOCBP and male subjects who are sexually active with
WOCBP on the importance of pregnancy prevention and the implications of an unexpected
pregnancy Investigators shall advise WOCBP and male subjects who are sexually active
with WOCBP on the use of highly effective methods of contraception. Highly effective
methods of contraception have a failure rate of < 1% when used consistently and
correctly.

At a minimum, subjects must agree to the use of one method of highly effective
contraception as listed below:

HIGHLY EFFECTIVE METHODS OF CONTRACEPTION

- Male condoms with spermicide

- Hormonal methods of contraception including combined oral contraceptive pills,
vaginal ring, injectables, implants and intrauterine devices (IUDs) such as
Mirena® by WOCBP subject or male subject's WOCBP partner.

- Female partners of male subjects participating in the study may use hormone based
contraceptives as one of the acceptable methods of contraception since they will
not be receiving study drug,

- IUDs such as ParaGard®,

- Tubal ligation

- Vasectomy.

- Complete Abstinence* *Complete abstinence is defined as complete avoidance of
heterosexual intercourse and is an acceptable form of contraception for all study
drugs. Acceptable alternate methods of highly effective contraception must be
discussed in the event that the subject chooses to forego complete abstinence

2. Acute co-existing proximal DVT (popliteal, femoral, iliac veins or IVC), pulmonary
embolism, splanchnic vein thrombosis, cerebral venous sinus thrombosis within the past
3 months for whom anticoagulation therapy is indicated.

3. Age < 18 years.

4. Continuous treatment with therapeutic anticoagulant for more than 72 hours
pre-randomization.

5. Contraindication to anticoagulant therapy

6. Significant kidney disease. Creatinine clearance < 25 ml/min using the Cockcroft-Gault
equation: glomerular filtration rate (GFR) = (140-age) * (Wt in kg) * (0.85 if female)
/ (72 * Cr). (within last four weeks)

7. Significant liver disease (e.g. acute hepatitis, chronic active hepatitis, cirrhosis)
or alanine transaminase (ALT) (or AST) > 3 x upper limit of normal (ULN). (within last
four weeks)

8. Platelet count < 50 x109/L.(within last four weeks)

9. Life expectancy < 12 months.

10. Current active bleeding.

11. Concomitant use of strong CYP3A4 inhibitors (e.g., HIV protease inhibitors, systemic
ketoconazole) or strong CYP3A4 inducers like rifampicin.

12. Active cancer defined as any evidence of cancer on cross-sectional imaging or cancer
treatments within the past 6 months (chemotherapy, radiation therapy or cancer related
surgery).

13. . Anticipated need for urgent/emergent surgery or major invasive procedure.

14. Dual antiplatelet therapy (thienopyridine plus aspirin) and/or aspirin greater than
165 mg while on study medication.