A Phase I Study of SB26 in Healthy Volunteers

The study includes two Parts; Part 1 includes the FiH exposure and SRD and Part 2 is the MRD.
Approximately 58 subjects will be enrolled in the study. New subjects will be recruited for
each cohort in both Parts. The SRD Part will include 5 or more dose levels and the MRD Part
will include 3 or more dose levels; additional dose level(s) may be added based on emerging
safety and PK data from prior cohorts.

Inclusion Criteria:

1. In the opinion of the Investigator, the subject is capable of understanding and
complying with protocol requirements.

2. The subject signs and dates a written informed consent form (ICF) and any required
privacy authorization prior to the initiation of any study procedures.

3. The subject is willing to comply with study procedures and restrictions.

4. The subject is a healthy adult man or woman of non-childbearing potential.

5. The subject is aged 18 to 65 years, inclusive, at the time of informed consent.

6. The subject weighs at least 50 kg and has a body mass index from 18 to 32 kg/m2,
inclusive, at Screening.

7. If the subject is a male who is non-sterilized and who is sexually active with a
female partner of childbearing potential, agrees to use adequate contraception from
signing of ICF throughout the duration of the study until 60 days (i.e., estimated > 5
half-lives) after the last dose of study drug(s).

8. The subject is a non-smoker or ex-smoker who has not used tobacco- or
nicotine-containing products (e.g., nicotine patch) for at least 6 months prior to
first administration of study drug (Day 1) and who has had a negative urine cotinine
at Screening and Check-in (Day -1).

Exclusion Criteria:

1. The subject has received any investigational compound or medication within 30 days or
five half-lives, whichever is the longest, prior to the first intended dose of study
drug.

2. The subject is a study site employee, immediate family member thereof, or is in a
dependent relationship with a study site employee who is involved in the conduct of
this study (e.g., spouse, parent, child, or sibling) or may consent under duress.

3. The subject has a known hypersensitivity to any component of the formulation of SB26,
or has had clinically significant infusion-related reactions to any prior biologic
drug unless it can be established that the reaction was due to components not present
in the formulation of SB26.

4. The subject has a positive urine result for drugs of abuse at Screening or Check-in
(Day -1).

5. The subject has a history of drug abuse or a history of alcohol abuse (defined as
drinking alcoholic beverages of more than 21 units per week for males and 14 units per
week for females; 1 unit = 14 g of pure alcohol, e.g., 1 unit = 250 mL of beer, 25 mL
of spirits or one glass [125 mL] of wine) within 1 year prior to Screening.

6. If male, the subject intends to father a child or to donate sperm during the course of
this study until 60 days after the last dose of study drug.

7. The subject has evidence of current or recent (within 6 months prior to Screening)
disease that, in the opinion of the Investigator, may pose additional risks to the
subject or confound the assessment of safety and tolerability. This should be
discussed with the Sponsor's medical representative if there is uncertainty about the
suitability of the subject.

8. The subject has a history of cancer, except basal cell carcinoma or cervical carcinoma
in situ that has been treated and in remission for at least 5 years prior to
Screening.

9. The subject has a positive test result for hepatitis B surface antigen, hepatitis C
virus antibody or human immunodeficiency virus at Screening.

10. The subject has poor peripheral venous access at Screening or Check in (Day -1).

11. The subject has donated or lost 450 mL or more of his or her blood volume (including
plasmapheresis) in the 30 days prior to Screening.

12. The subject has an electrocardiogram (ECG) showing a clinically significant
abnormality at Screening or Check-in (Day -1). Entry of any subject with an abnormal
but not clinically significant ECG must be approved, and documented by signature of
the Principal Investigator or a medically qualified sub-Investigator.

13. The subject's ECG has a QT interval with Fridericia correction method > 450 msec for
male, > 470 msec for female or a PR interval outside the range 120 to 220 msec,
confirmed on repeat testing within a maximum of 30 minutes, at Screening or Check-in
(Day -1).

14. The subject has a sustained resting heart rate outside the range 40 to 100 beats per
minute, confirmed on repeat testing within a maximum of 30 minutes, at Screening or
Check-in (Day -1).

15. The subject has systolic blood pressure > 140 or < 90 mmHg or a diastolic blood
pressure > 90 or < 50 mmHg at Screening or Check-in (Day -1). One repeat testing is
allowed at Screening and Check-in (Day -1)

16. The subject has any other abnormal laboratory values at Screening or Check-in (Day
-1), confirmed upon repeat testing, that suggest a clinically significant underlying
disease per the Investigator.