SAFEGUARD

This is a Phase 2b, investigator* and participant-blinded, placebo-controlled, parallel-arm study to evaluate the efficacy, safety and tolerability of SAB 142 in patients with Stage 3 New Onset of Type 1 Diabetes (NOT1D).

Inclusion Criteria:

1. Participant and/or appropriate legal guardian must have given written informed consent and/or assent according to local, regional and/or country specific guidance before any study-related activities are carried out and must be able to understand the full nature and purpose of the trial, including possible risks and adverse effects.

2. Males and females 15-40 years old at the time of randomisation in Part A. Males and females 5-40 years old*, inclusive, at the time of randomisation in Part B.

3. Weight ≥16. 0 kg at time of randomisation.

4. Participant has received a diagnosis of T1D according to American Diabetes Association criteria within 100 days of randomization. For participants who were initially misdiagnosed with Type 2 diabetes, time from misdiagnosis with Type 2 diabetes to randomization is 100 days. Note: The date of diagnosis is defined as the date of the first insulin dose or any other glucose lowering medication. An extension of no more than 14 days is permitted if a participant has planned and/or is required to receive a vaccination within 30 days prior to randomisation or is completing the 10 day CGM period.

5. Participant has random C-peptide levels of ≥0. 2 nmol/L, measured during Screening. One random C-peptide retest during screening period is allowed.

6. Participant completed all scheduled samples for C-peptide collected during the MMTT test during Screening.

7. Participant has a positive result on testing for at least one of the following T1D-related autoantibodies during screening:

   • Glutamic acid decarboxylase 65 (GAD65)

   • Islet antigen 2 (IA-2)

   • Zinc transporter 8 (ZnT8)

   • Insulin autoantibodies (if testing within the first 14 days of insulin treatment)

8. Female participants: a. Must be of nonchildbearing potential, i.e., pre-pubertal*, surgically sterilised (hysterectomy, bilateral salpingectomy, bilateral oophorectomy) at least 6 weeks before the screening, or postmenopausal (where postmenopausal is defined as no menses for 12 months without an alternative medical cause and a follicle stimulating hormone (FSH) level consistent with postmenopausal status, per local laboratory guidelines), or b. If of childbearing potential, must: i. Have a negative result on a serum (beta human chorionic gonadotropin [β-HCG]) at screening and a negative urine β-HCG pregnancy test prior to study drug administration on Day 1 of both treatment periods.

   ii. Agree not to become pregnant or donate ova from signing the consent form until the end of study visit.

   iii. If not exclusively in a same-sex relationship or abstinent as a committed lifestyle, must agree to use adequate contraception (which is defined as use of a condom by the male partner combined with use of a highly effective method of contraception from signing the consent and for the duration of the study.

   • Note: Female participants will be considered to be pre-pubertal (and of nonchildbearing potential) if they have not yet started menstruation. This should also be verified by the parent(s)/guardian(s). If a female participant reaches menarche during the study, then she is to be considered as a woman of childbearing potential from that time forwards, and contraceptive requirements will apply.

9. Male participants, if not biologically or surgically sterilised, must:

   1. Agree not to donate sperm from signing the consent form until EOS.

   2. If engaging in sexual intercourse with a female partner who could become pregnant, agree to use adequate contraception (defined as use of a condom combined with use of a highly effective method of contraception from signing the consent form until EOS.

   3. If engaging in sexual intercourse with a female partner who is not of childbearing potential or a same-sex partner, agree to use a condom from signing the consent form until EOS.

10. Prior to receiving study drug, participant must agree to receive locally, regionally

and/or country-specific required age-appropriate immunisations. Participants are

advised but not required to comply with the guidelines for immunosuppressed

individuals and those with chronic disease (diabetes mellitus) according to current

local, regional and/or country* specific guidelines. Note: Vaccines are permitted

within the timeframes specified in exclusion criterion #17.

1. Participant agrees not to receive other forms of experimental treatment from the

time of signing informed consent and for the duration of the study, particularly

agents that may be immune modulatory in nature and/or stimulate pancreatic β cell

regeneration or insulin secretion.

1. Participant has suitable venous access for blood sampling.

2. Participant is willing and able to comply with all study assessments and adhere to

the protocol schedule and restrictions.

Exclusion Criteria:

1. Participant has known allergy, hypersensitivity or moderate to severe allergic reaction including anaphylaxis to natural or recombinant antibodies, biologic treatments, passive vaccines, pork, or any other component of the study drug formulation (including biologic medications).

2. Participant has a known allergy or hypersensitivity to any of the protocol-required concomitant medications.

3. Participant has been an active participant in a therapeutic drug, invasive medical device, or vaccine clinical trial within 12 weeks before Screening Visit (SV)2.

4. Participant has received teplizumab or any investigational immunomodulatory anti-CD3 treatment within any timeframe prior to screening.

5. Participant has a significant uncontrolled renal, cardiac, vascular, pulmonary, gastrointestinal, neurologic, haematologic, rheumatologic, oncologic, psychiatric, or immune deficiency that may interfere with the participant's safely participating in the study or with interpretation of the safety and/or efficacy profile of investigational medicinal product (IMP). For any disorders, a participant with a stable, well-controlled condition that is not felt to interfere with study participation may be enrolled.

6. Participant has any autoimmune disease other than T1D (e.g., latent autoimmune diabetes in adults, rheumatoid arthritis, polyarticular juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, multiple sclerosis, systemic lupus erythaematous) that is currently managed with systemic immunotherapy, with the exception of clinically stable thyroid or celiac disease.

7. Participant is prone to infections, or has chronic, recurrent or opportunistic infectious disease, including but not limited to renal, respiratory or skin infections, Pneumocystis carinii, aspergillosis, latent or active granulomatous infection, histoplasmosis, or coccidioidomycosis.

8. Participant has a history of or serologic evidence at screening of current or past infection with human immunodeficiency virus (HIV)-1 or 2, hepatitis B virus (HBV), or hepatitis C virus (HCV) antibodies.

9. Evidence of active or latent tuberculosis (TB) as documented by medical history and examination, chest X-rays (posterior anterior and lateral), and/or TB testing. Note: Blood testing (e.g., QuantiFERON® TB Gold test) is strongly preferred; if not available, any local approved TB test is allowed.

10. Serious systemic viral, bacterial, or fungal infection (e.g., pneumonia,

pyelonephritis), infection requiring hospitalization or IV anti-infective treatments

or significant acute or chronic viral (including history of recurrent or active

herpes zoster, acute or active cytomegalovirus [CMV], Epstein-Barr Virus [EBV] as

determined at screening), bacterial, or fungal infection (e.g., osteomyelitis) 30

days before and during screening. Note: Participants with confirmed active EBV or

CMV infection based on polymerase chain reaction (PCR) test can be retested;

asymptomatic participants with the most recent PCR-negative test are eligible for

participation. Participants with an active mild infection at Screening may be

enrolled once the symptoms have resolved and all I/E are met. Participants who have

an active infection and/or fever ≥38.0°C (100.4°F) within the 48 hours prior to dose

administration should not be dosed.

1. Participant has a diagnosis of significant liver disease or at screening ALT and/or

AST >2× or total bilirubin of >1.5× of the age* and sex-specific upper limit of

normal (ULN) according to the central laboratory and confirmed by repeated tests.

Liver function tests can be repeated during screening and if normalised, participant

maybe eligible for randomization. Note: Participants with Gilbert's syndrome are

allowed to enrol if only total and/or indirect bilirubin are elevated above ULN

while ALT, AST, and alkaline phosphatase (ALP) are within the normal laboratory

ranges.

1. An individual has any of the following haematologic parameters, confirmed by repeat

tests, during Screening:

• Lymphocyte count: