A Randomized, Double-blind, Study to Explore the Effect of GED-0301 in Subjects With Active Crohn's Disease

Approximately 51 subjects will be randomized in a 1:1:1 ratio to receive 1 of 3 treatment
regimens in a 12-week Induction Phase:

GED-0301 160 mg Once Daily (QD) for 12 weeks GED-0301 160 mg Once Daily (QD) for 8 weeks
followed by 4 weeks of placebo GED-0301 160 mg Once Daily (QD) for 4 weeks followed by 8
weeks of placebo Treatment assignment at baseline will be stratified via an Interactive Voice
Response System (IVRS)/or an Interactive Web Response System (IWRS) based on previous
exposure to TNF-α blockers (yes/no) and disease location (disease restricted to the terminal
ileum and/or up to the mid transverse colon only, or disease involving at least 1 ulcerated
segment distal to mid transverse colon). The number of subjects with previous exposure to
TNF-α blockers is targeted to be approximately 40%. The number of subjects with disease
involving distal to mid transverse colon is targeted to comprise approximately 50% of the
study population.

The study will consist of 5 phases:

Screening Phase - up to 4 weeks Induction Phase - 12 weeks Eligible subjects will enter the
Induction Phase at the Baseline Visit (Week 0/Induction Visit 1). Subjects will be assigned
randomly to receive IP as described above.

At Induction Week 12, subjects (responders) who achieve clinical remission, defined as a CDAI
score < 150, or clinical response, defined as a decrease from baseline of ≥ 100 points in
Crohn's Disease Activity Index (CDAI) score, at any of the following Induction Visits (Weeks
4, 8 and/or Week 12) will enter the Observation Phase. The Observation Phase will have a
duration of up to 52 weeks. Subjects who are unable to achieve clinical remission or clinical
response (no responders) at the following Induction Visits (Weeks 4, 8 and Week 12), will be
discontinued from the study. Subjects who enter the Observation Phase and were receiving
corticosteroids at baseline will start tapering corticosteroids at the end of the Induction
Phase (Induction Week 12).

Observation Phase - up to 52 weeks Subjects who enter the Observation Phase will be evaluated
by CDAI score every 4 weeks. Subjects will not receive investigational product (IP) during
the Observation Phase. Subjects who experience a partial loss of response or are unable to
taper corticosteroids during the Observation Phase will enter the Extension Phase. Partial
loss of response is defined as 2 consecutive visits with both a CDAI score ≥ 150 and an
increase of CDAI score ≥ 50 points from the CDAI score at the visit when the subject was
first a responder during the Induction Phase. Partial loss of response must be confirmed 2 to
4 weeks post initial identification of partial loss of response. Subjects who do not
experience a partial loss of response until Observation Week 52 will have an end-of-study
visit.

Extension Phase -24 weeks Subjects who enter the Extension Phase will receive GED-0301 40 mg
QD on a 4-week, alternating dosing schedule (4 weeks of treatment with GED-0301, followed by
4 weeks without GED-0301 treatment) for 24 weeks.

Follow-up Phase - 4 weeks

Subjects who complete the Extension Week 24 Visit will have 2 options:

- Subjects will have the Follow-up Visit if they chose to not enter the Long-Term
Extension Study or it has not been initiated

- Subjects may proceed to the Long-Term Extension Study, provided this study has been
initiated by the time the subjects complete study GED-0301-CD-001 and subjects meet all
inclusion/exclusion criteria of the Long-Term Extension Study.

Subjects who prematurely discontinue from the study, for any reason, will enter the Follow-up
Phase, the 4-week period after the last study visit.

Inclusion Criteria:

1. Is a male or female who is ≥18 years at the time of signing the Informed Consent Form
(ICF).

2. Understand and voluntarily sign an Informed Consent Form (ICF) prior to conducting any
study related assessments/procedures.

3. Able to adhere to the study visit schedule and other protocol requirements.

4. Diagnosis of Crohn's Disease (CD) with a duration of at least 3 months prior to
screening.

5. Diagnosis of ileitis, ileocolitis or colitis , as determined by endoscopic,
radiographic or any other imaging modality (eg, magnetic resonance imaging [MRI],
computed tomography [CT] scan) evaluation performed within 2 years prior to screening.
Subjects with colitis restricted to the left colon will not be allowed in the trial.

6. Active disease, defined as Crohn's Disease Activity Index (CDAI) score ≥ 220 and ≤ 450
(range: 0 to 600) at screening.

7. Simple Endoscopic Score for Crohn's Disease (SES-CD) score ≥ 7 at screening. Subjects
with ileitis only will require Simple Endoscopic Score for Crohn's Disease (SES-CD) ≥
4

8. Must have failed or experienced intolerance to at least one of the following:

aminosalicylates, budesonide, systemic corticosteroids, immunosuppressants (ie, 6
mercaptopurine [6-MP], azathioprine [AZA], or methotraxate [MTX]) or tumor necrosis
factor-α tumor necrosis factor-α (TNF-α) blockers (eg, infliximab, adalimumab or
certolizumab) .

9. Subjects receiving oral aminosalicylates may continue their use during the study,
provided that dose has been stable for at least 2 weeks prior to screening. The dose
of oral aminosalicylates must remain stable through the duration of the study or early
termination from the study. If oral aminosalicylates have been recently discontinued,
treatment must have been stopped at least 2 weeks prior to screening.

10. Subjects receiving oral corticosteroids may continue their use during the Induction
Phase, provided that the dose (prednisone ≤ 20 mg/day or equivalent, budesonide ≤ 9
mg/day) has been stable for 3 weeks prior to screening. If oral corticosteroids were
recently discontinued, discontinuation must have been completed at least 4 weeks prior
to screening. Corticosteroid doses should remain stable until the subject is eligible
to start corticosteroids tapering.

11. Subjects receiving immunosuppressants, such as , 6 mercaptopurine (6-MP), azathioprine
(AZA), or methotraxate (MTX) may continue their use during the study, provided that
treatment was initiated ≥ 12 weeks prior to screening. The dose of immunosuppressants
must be at a stable dose for ≥ 8 weeks prior to the Baseline Visit and must remain
stable through the duration of the study or early termination from the study. Subjects
who discontinued immunosuppressants should have stopped them at least 8 weeks prior to
screening.

12. Must meet the following laboratory criteria:

1. White blood cell count ≥ 3000/mm3 (≥ 3.0 X 10^9//L) and < 14,000/mm3 (< 14.0 X
10^9/L)

2. Platelet count ≥ 100,000/mm3 (≥ 100 X 10^9/L)

3. Serum creatinine ≤ 1.5 mg/dL (≤ 132.6 μmol/L)

4. Aspartate aminotransferase (AST) / serum glutamic-oxaloacetic transaminase (SGOT)
and alanine aminotransferase (ALT) / serum glutamic-pyruvic transaminase (SGPT) ≤
2 X upper limit of normal (ULN)

5. Total bilirubin ≤ 2 mg/dL (≤ 34 μmol/L) unless there is a confirmed diagnosis of
Gilbert's disease

6. Hemoglobin ≥ 9 g/dL (≥ 5.6 mmol/L)

7. Activated partial thromboplastin time (APTT) ≤ 1.5 X ULN

13. Females of childbearing potential (FCBP) must have a negative pregnancy test at
Screening and the Baseline Visit. While on IP and for at least 28 days after the Early
Termination Visit or the end-of-study visit (Observation Week 52 or Extension Week
24), FCBP who engage in activity in which conception is possible must use 1 of the
approved contraceptive options2 described below: Option 1: Any one of the following
highly effective methods: hormonal contraception (for example, birth control pills,
injection, implant, transdermal patch, vaginal ring); intrauterine device (IUD); tubal
ligation (tying your tubes); or a partner with a vasectomy OR

Option 2: Any two of the following effective methods: male or female condom PLUS one
of the following additional barrier methods:

1. diaphragm with spermicide;

2. cervical cap with spermicide; or

3. contraceptive sponge with spermicide

14. Male subjects (including those who have had a vasectomy) who engage in activity in
which conception is possible must use barrier contraception (male latex condom or
nonlatex condom NOT made out of natural [animal] membrane [for example, polyurethane])
while on Investigational Product (IP) and for at least 28 days after the Early
Termination Visit or the end-of-study visit (Observation Week 52 or Extension Week
24).

Exclusion Criteria:

1. Diagnosis of Crohn's colitis restricted to the left colon , ulcerative colitis (UC),
indeterminate colitis, ischemic colitis, microscopic colitis, radiation colitis or
diverticular disease-associated colitis.

2. Local manifestations of Crohn's Disease (CD) such as strictures, abscesses, fistula,
short bowel syndrome or other disease complications for which surgery might be
indicated or could confound the evaluation of efficacy.

3. Intestinal resection within 6 months or any intra-abdominal surgery within 3 months
prior to screening.

4. Subjects with an ileostomy or a colostomy.

5. Stool positive for any enteric pathogen or C. difficile toxin at screening.

6. History of colorectal cancer or colorectal dysplasia.

7. Prior use of mycophenolic acid, tacrolimus, sirolimus, cyclosporine, thalidomide or
apheresis (eg, Adacolumn) for the treatment of CD. In addition, prior use of any of
these treatment modalities for an indication other than CD within 8 weeks of screening
is also excluded.

8. Use of intravenous (IV) corticosteroids within 2 weeks of screening.

9. Use of topical treatment with 5 aminosalicylic acid (5-ASA) or corticosteroid enemas
or suppositories within 2 weeks of screening

10. Use of antibiotic therapy for the treatment of Crohn's Disease (CD) within 3 weeks of
screening.

11. Use of cholestyramine within 3 weeks of screening.

12. Prior treatment with more than 2 tumor necrosis factor-α (TNF-α) blockers.

13. Prior treatment with any integrin antagonists (eg, natalizumab or vedolizumab).

14. Use of tumor necrosis factor-α (TNF-α) blockers within 12 weeks of the screening

15. Administration of total parenteral nutrition (TPN) within 4 weeks of screening.

16. History of any clinically significant neurological, renal, hepatic, gastrointestinal,
pulmonary, metabolic, cardiovascular, psychiatric, endocrine, hematological disorder
or disease, or any other medical condition that, in the Investigator's opinion, would
prevent the subject from participation in the study.

17. Any condition, including the presence of laboratory abnormalities, which places the
subject at unacceptable risk if he/she was to participate in the study or confounds
the ability to interpret data from the study.

18. Pregnant or breastfeeding.

19. History of any of the following cardiac conditions within 6 months of screening:
myocardial infarction, acute coronary syndrome, unstable angina, new onset atrial
fibrillation, new onset atrial flutter, second- or third-degree atrioventricular
block, ventricular fibrillation, ventricular tachycardia, heart failure, cardiac
surgery, interventional cardiac catheterization (with or without a stent placement),
interventional electrophysiology procedure, or presence of implanted defibrillator.

20. Known active current or history of recurrent bacterial, viral, fungal, mycobacterial
or other infections (including but not limited to tuberculosis and atypical
mycobacterial disease and Herpes zoster), human immunodeficiency virus (HIV), or any
major episode of infection requiring hospitalization or treatment with intravenous
(IV) or oral antibiotics within 4 weeks of screening.

21. History of congenital or acquired immunodeficiency (eg, common variable
immunodeficiency disease).

22. History of malignancy, except for:

1. Treated (ie, cured) basal cell or squamous cell in situ skin carcinomas

2. Treated (ie, cured) cervical intraepithelial neoplasia or carcinoma in situ of
the cervix with no evidence of recurrence within the previous 5 years

23. Subjects who have received any investigational drug or device within 1 months of
screening.

24. Prior treatment with GED-0301, or participation in a clinical study involving
GED-0301.

25. History of alcohol, drug, or chemical abuse within the 6 months prior to screening.

26. Known hypersensitivity to oligonucleotides or any ingredient in the IP.