Efficacy and Safety of TY027, a Treatment for COVID-19, in Humans

Phase 3

Terminated

• Conditions: Coronavirus Disease-2019 (COVID-19)
• Interventions: Other: 0.9% saline; Biological: TY027

• Registration Number: NCT04649515
• Lead Sponsor: Tychan Pte Ltd.

Brief Summary

The emergence \& rapid spread of the coronavirus disease 2019 (COVID-19) since December 2019 across 188 countries globally has become a major public health crisis. COVID-19 was declared a pandemic by the World Health Organisation on 11 March 2020. To date, tens of millions of cases have been reported and over 3% of these cases have died. COVID-19 is an acute respiratory disease caused by the novel SARS-CoV-2 virus from the Betacoronavirus genus, just like SARS-CoV and MERS-CoV. SARS-CoV-2 is primarily transmitted person-to-person through respiratory droplets/close contact. Fomite transmission has also been shown as a transmission route. Common respiratory symptoms such as fever, sore throat, cough \& shortness of breath, may appear 2 - 14 days after exposure. About 20% of infected cases progress to severe disease resulting in an estimated 2 - 5% mortality rate. With the unrelenting increase in cases being reported worldwide, there is thus an urgent need for therapeutics to be developed to treat disease \& reduce further transmission in order to disrupt the ongoing pandemic.

To date, there are no specific proven antiviral treatment to prevent disease progression from mild to severe respiratory dysfunction among COVID-19 patients. Supportive care is recommended for symptom relief \& for severe cases. Numerous vaccine candidates against SARS-CoV-2 are under development. Tychan's TY027, a fully engineered human IgG, is one of the first few biologics in the world, specifically targeting SARS-CoV-2, to enter human clinical trials. Preliminary data from our phase 1 healthy volunteer trial (SCT-001; ClinicalTrials.gov Identifier NCT04429529) reveals that TY027 is safe \& well-tolerated up to 20 mg/kg tested. A total of 10 adverse events (AEs) were observed, all were of mild in intensity with none resulting in subject withdrawal from the study. There were no serious adverse events \& no clinically relevant trends in mean clinical laboratory, physical examinations, vital signs or ECG results were observed. Pharmacokinetic profile of subjects across dose cohorts 1 - 4, up to Day 14, were comparable to those typical of human IgG1 antibody with serum concentrations declining in a biphasic manner. Exposure of TY027, based on Cmax, increased in a linear \& generally dose proportional manner. It is anticipated that TY027, when administered to acutely infected COVID-19 patients, could reduce disease severity. It may potentially also be used as a prophylaxis against COVID-19 amongst high risk contacts.

Detailed Description

This is a Phase 3 Multi-Site, Randomised, Placebo Controlled, Double Blind, Single Dose Study of TY027 for Early Treatment of COVID-19.

Efficacy and safety of single dose IV infusion of TY027 in COVID-19 patients will be assessed.

A total of 1,305 COVID-19 patients will be enrolled. The first 15 patients will be randomised 1:1:1 to receive either (i) a single fixed dose of 1,500 mg TY027, (ii) a single fixed dose of 2,000 mg TY027 or (iii) Placebo (N = 5 per group) for initial safety assessment. This safety assessment will comprise the safety review of clinical signs, adverse events (AEs) and laboratory test results up to Day 3 post-dose.

Subsequent patients will be randomised 1:1 to receive either a single fixed dose of 2,000 mg TY027 (2,000 mg TY027 group) or Placebo (Placebo group) (N = 645 per group).

All patients will be inpatient for up to 7 days post-dosing and followed up on Days 14 and 28.

If a patient becomes clinically well enough for discharge before Day 7, at the discretion of attending physician, collection of subsequent events/parameters such as abbreviated physical examinations, vital signs, clinical laboratory assessments, pharmacodynamic assessment, biomarker assessment, disseminated intravascular coagulation assessment scheduled after discharge will no longer be feasbile. Conversely, if a patient was to be hospitalised beyond 7 days for medically indicated reasons, daily monitoring and medical assessment will continue, with any additional ad hoc sampling to be recorded as unscheduled visit(s).

Remote monitoring through a telephone or video call will be performed on days post-discharge as per originally scheduled in schedule of events, as well as on Day 14 while patients are serving their quarantine order or has been discharged home.

All discharged patients are to contact the Principal Investigator or the study team as soon as possible should they experience a worsening of their condition, or if they are admitted to hospital for COVID-19-related symptoms, before their Day 28 visit.

Final safety and efficacy analysis of all patients will be assessed at the end of the study.

Study Timeline

• Study First Submitted: 2020-11-26
• Study First Submitted QC: 2020-11-30
• Study First Posted: 2020-12-02
• Study Start: 2020-12-04
• Status Verified: 2022-03
• Primary Completion: 2022-03-04
• Study Completion: 2022-03-04
• Last Update Submitted: 2022-03-08
• Last Update Posted: 2022-03-24

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 17

Inclusion Criteria

1. Symptomatic and RT-PCR confirmed COVID-19 within 6 days from symptom onset.

2. Has any one of the following factors associated with disease progression:

   1. Elevated lactate dehydrogenase (LDH)
   2. Elevated C reactive protein (CRP)
   3. Lymphocyte count below normal limit
   4. Age 40 and above
   5. History of well-controlled diabetes, hypertension, chronic obstructive lung disease or ischemic heart diseases
   6. Stable chronic renal disease
   7. History of asthma

3. Disease outcome score of 6, 7 or 8 based on the COVID Scale

4. Willing to comply with the requirements of the study protocol and attend scheduled study visits

5. Can give written informed consent approved by the Ethical Review Board governing the site

Exclusion Criteria

1. Aged below 21 years old

2. Female who is pregnant or breast-feeding

3. With the following conditions, but not limited to:

   1. Known or suspected congenital or acquired immunodeficiency; or receipt of immunomodulation therapy such as anti-cancer chemotherapy or radiation therapy; or long-term systemic corticosteroid therapy defined as prednisone or equivalent for more than 2 consecutive weeks within the past 3 months
   2. Child-Pugh Class C chronic liver disease
   3. Renal insufficiency with an estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73m2 calculated by the CKD-EPI formula
   4. Suspected or confirmed active bacterial, fungal or mycobacterial infection

4. History of any allergic reaction to monoclonal antibodies

5. Currently enrolled in another COVID-19 investigational drug study

6. Previously enrolled in a COVID-19 investigational vaccine study

7. Any medical condition, which in the opinion of the Investigator, will compromise the safety of the patient

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo	0.9% saline	Placebo will be administered via IV infusion over a period of 30 minutes.
TY027 1,500 mg	TY027	1,500 mg of TY027 will be administered via IV infusion over a period of 30 minutes.
TY027 2,000 mg	TY027	2,000 mg of TY027 will be administered via IV infusion over a period of 30 minutes.

Primary Outcome Measures

Name	Time	Method
To evaluate the efficacy of a single dose intravenous (IV) infusion of TY027 in reducing disease progression, defined as progression to score 4 and below on COVID scale	Within the first 14 days	Proportion of COVID-19 patients with disease progression, defined as progression to score 4 and below on the COVID Scale, within the first 14 days after a single dose IV infusion of TY027 as compared to placebo

Secondary Outcome Measures

Name	Time	Method
All cause mortality rate	28 days	All cause mortality rate by Day 28 in COVID-19 patients who receive a single dose IV infusion of TY027 as compared to placebo
Proportion of subjects in categories 4, 3, 2 and 1 of the COVID scale	Up to Day 28	Proportion of subjects in categories 4, 3, 2 and 1 of the COVID scale at Day 7, Day 14 and Day 28
Proportion of COVID-19 patients with a minimum of 0.5 log time-weighted viral load reduction from saliva samples, via sub-genomic qRT-PCR	Day 7 post-dose or day of discharge, whichever is earlier	Proportion of COVID-19 patients with a minimum of 0.5 log time-weighted viral load reduction from saliva samples, via sub-genomic qRT-PCR, at Day 7 post-dose or day of discharge, whichever is earlier, as compared to baseline between study groups
Proportion of COVID-19 patients tested negative for SARS-CoV-2 via reverse transcriptase-polymerase chain reaction (RT-PCR)	Up to Day 28	Proportion of COVID-19 patients tested negative for SARS-CoV-2 via reverse transcriptase-polymerase chain reaction (RT-PCR) at Day 3, Day 5, Day 7, Day 14 and Day 28 after a single dose IV infusion of TY027 as compared to placebo
Rate of AEs (grade 3 and above) and SAEs in COVID-19 patients	28 days	Rate of AEs (grade 3 and above) and SAEs in COVID-19 patients after a single dose IV infusion of TY027 as compared to placebo
Number of days COVID-19 patients require supplemental oxygen, high flow oxygen, non-invasive and invasive mechanical ventilation (if applicable)	28 days	Number of days COVID-19 patients require supplemental oxygen, high flow oxygen, non-invasive and invasive mechanical ventilation (if applicable) after a single dose IV infusion of TY027 as compared to placebo up to Day 28

Trial Locations

Locations (1)

Singapore General Hospital; 🇸🇬 Singapore, Singapore