Clinical Study to Evaluate Efficacy and Safety of ALLO-ASC-DFU in Patients With Diabetic Wagner Grade 2 Foot Ulcers.

Inclusion Criteria:

1. Subject is between 19 and 75 years of age.

2. Subject is diagnosed with Type I or Type II diabetics.

3. Diabetic foot ulcer has been more than 4 weeks but less than 52 weeks at thescreening visit.

4. Ulcer located in the foot and ulcer size is between 1.5~15 cm2.

5. Ulcer graded 2 by Wagner grade.

6. Foot ulcer extended to ligament, tendon, joint capsule, fascia, muscle andperiosteum.

7. Ulcer is free of necrotic debris.

8. Ulcer area blood circulation meets one of the following criteria;

• Blood vessels around the ulcer detected by Doppler Test

• Range of Ankle Brachial Index (ABI) is > 0.7 to < 1.3

• Transcutaneous Oxygen Pressure (TcPO2) > 30mmHg or Toe Blood Pressure (TBP) > 40mmHg.

• Skin Perfusion Pressure (SPP) > 30mmHg

9. Subject is able to give written informed consent prior to study start and willing tocomply with the study requirements.

Exclusion Criteria:

1. Ulcer is of non-diabetic pathophysiology.

2. There is gangrene in any part of the target foot ulcer.

3. The longest dimension of the target foot ulcer exceeds 15 cm at the enrollmentvisit.

4. Other wounds within 2cm of the target foot ulcer.

5. The ulcer has increased or decreased in size by ≥ 30% during two weeks after thescreening visit.

6. Patient requiring intravenous (IV) antibiotics to treat foot wound infection at thescreening and enrollment visit.

7. Current evidence of active charcot on the study foot, osteomyelitis, cellulitis, orevidence of other infection including fever or purulent drainage from wound site.

8. Patient with skin lesion confirmed by biopsy (when Investigator deems suspicious)and then judged by Investigator to be an etiology other than diabetic foot ulcer.

9. An active malignant tumor(malignant melanoma, squamous cell carcinoma, basal cellcarcinoma) on the body or skin.

10. Have a glycated hemoglobin A1c (HbA1c) level of > 14%

11. Have random blood sugar > 450mg/dL

12. Have severe renal failure with creatinine > 3.0mg/dL.

13. Have severe hepatic deficiencies

• Total bilirubin ≥ 1.5×upper normal limit(UNL)

• AST, ALT ≥ 2.0×UNL

• Serum albumin < 2.0mg/dL

14. Is Human Immunodeficiency Virus (HIV) positive

15. Have a known history of allergic or hypersensitive reaction to bovine-derivedproteins or fibrin glue

16. Pregnant or breast-feeding.

17. Is unwilling to use an acceptable method of birth control during the whole study.

18. Have a clinically relevant history of alcohol or drugs abuse at the screening visit.

19. Is not able to understand the objective of the study or to comply with the studyrequirements

20. Is considered by the Investigator to have a significant disease which might impactthe study

21. Is considered not suitable for the study by Investigator

22. Have a history of malignancy within the last 5 years (except carcinoma in situ)

23. Is currently or were enrolled in another clinical study within 60 days of screening

24. Have undergone wound treatments with growth factors, dermal substitutes, or otherbiological therapies within the last 30 days.

25. Is receiving oral or parenteral corticosteroids, any immunosuppressive, or cytotoxicagents with unstable dose within the last 30 days

26. Cannot maintain off-loading process and device.