A Randomized, Double-Blind, Parallel-Group, Vehicle-Controlled, Multicenter Study Comparing Diclofenac Sodium Gel, 3% to Solaraze® Gel, 3% in the Treatment of Actinic Keratosis on the Face or Bald Scalp

Inclusion Criteria:

- Willing and able to provide written informed consent for the study.

- At least 18 years of age

- Immunocompetent male or nonpregnant and nonlactating female. Each female subject of
childbearing potential (excluding women who are surgically sterilized or
postmenopausal for at least 2 years), in addition to having a negative urine
pregnancy test at Visit 1/Day 1, must be willing to use an acceptable form of birth
control during the study. For the purpose of this study, the following are considered
acceptable methods of birth control: oral contraceptives, contraceptive patches,
contraceptive implant, vaginal contraceptive, double-barrier methods (e.g., condom
and spermicide), contraceptive injection (Depo-Provera®), intrauterine device IUD
(Mirena®), Essure®, and abstinence with a documented second acceptable method of
birth control if the subject becomes sexually active.

- Clinical diagnosis of AK, defined as ≥ 5 and ≤ 10 clinically typical, visible,
discrete, nonhyperkeratotic, nonhypertrophic AK lesions, each at least 4 mm in
diameter, contained within a 25-cm2 treatment area on either the face or bald scalp,
but not both face and scalp.

- In general good health and free from any clinically significant disease, other than
AK, that might interfere with the study evaluations.

- Willing and able to understand and comply with the requirements of the study, apply
the study medication as instructed, attend the required visits, comply with therapy
prohibitions, and be able to complete the study.

Exclusion Criteria:

- Presence of active gastrointestinal ulceration or bleeding.

- Presence of severe renal or hepatic impairment.

- Presence of atopic dermatitis, basal cell carcinoma, eczema, psoriasis, rosacea,
squamous cell carcinoma, sunburn, or other possible confounding skin conditions on
the treatment area of either the face or bald scalp.

- Clinically significant systemic disease (immunological deficiencies), unstable
medical disorder, life-threatening disease, or current malignancies.

- Use within 6 months (180 days) prior to randomization of oral isotretinoin.

- Use within 6 months (180 days) prior to randomization on the face or bald scalp where
the designated treatment area is located of 1) chemical peel, 2) dermabrasion, 3)
laser abrasion, 4) PUVA (psoralen plus ultraviolet A) therapy, or 5) UVB therapy.

- Use within 6 months (180 days) prior to randomization of systemic cancer chemotherapy
medications.

- Use within 1 month (30 days) prior to randomization on the face of bald scalp where
the designated treatment are is located of 1) cryodestruction or chemodestruction, 2)
curettage, 3) photodynamic therapy, 4) surgical excision, 5) topical 5-fluorouracil,
6) topical corticosteroids, 7) topical diclofenac, 8) topical imiquimod, 9) topical
retinoids, 10) other treatments for actinic keratosis.

- Use within 1 month (30 days) prior to randomization of 1) immunomodulators or
immunosuppressive therapies, 2) interferon, 3) systemic (oral and injectable)
corticosteroids, 4) cytotoxic drugs. Intranasal or inhaled corticosteroids are
acceptable if kept constant throughout the study. Intra-articular injection of
steroids is acceptable for this study.

- Known hypersensitivity or allergies to diclofenac, benzyl alcohol, polyethylene
glycol monomethyl ether 359, hyaluronate sodium or any component of the study
medication (in any dosage form).

- Previous or current history of allergies to aspirin (ASA) or other NSAIDS.

- Females who are pregnant, breastfeeding, intending to become pregnant during the
study, or who do not agree to use an acceptable form of birth control during the
study.

- Any clinically significant condition or situation other than the condition being
studied that, in the opinion of the investigator, would interfere with the study
evaluation or optimal participation in the study.

- Use of any investigational drug or investigational device within 1 month (30 days)
prior to the randomization.

- Previous participation in this study.

- Current involvement in activities that require excessive or prolonged sun exposure.

- Consumption of excessive alcohol, abuse of drugs, or a condition that could
compromise the subject's ability to comply with study requirements.