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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT06402136




Registration number
NCT06402136
Ethics application status
Date submitted
2/05/2024
Date registered
7/05/2024
Date last updated
7/05/2024

Titles & IDs
Public title
Evaluation Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of 83-0060 in Healthy Volunteers
Scientific title
A Randomised, Double-Blind, Placebo-Controlled, First-in-Human Study of Orally Administered 83-0060 to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of 83-0060 in Healthy Volunteers
Secondary ID [1] 0 0
CT-2024-CTN-00084-1
Secondary ID [2] 0 0
83-0060-0001
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Healthy Volunteers Only 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - 83-0060
Treatment: Drugs - Placebo

Experimental: Single dose level 1 or placebo - Dose level 1. SAD study part.

Experimental: Single dose level 2 or placebo - Dose level 2. SAD study part.

Experimental: Single dose level 3 or placebo - Dose level 3. SAD study part.

Experimental: Single dose level 4 or placebo - Dose level 4. SAD study part.

Experimental: Single dose level 5 or placebo - Dose level 5. SAD study part.

Experimental: Multiple dose level 1 or placebo - Dose level 1. MAD study part.

Experimental: Multiple dose level 2 or placebo - Dose level 2. MAD study part.


Treatment: Drugs: 83-0060
Oral MPro inhibitor

Treatment: Drugs: Placebo
Placebo
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Plasma concentration
Timepoint [1] 0 0
72 hours for SAD, 10 days for MAD
Secondary outcome [1] 0 0
Incidence of AEs
Timepoint [1] 0 0
8 days in SAD part, 17 days for MAD part
Secondary outcome [2] 0 0
Incidence of drug-related AEs
Timepoint [2] 0 0
8 days in SAD part, 17 days for MAD part
Secondary outcome [3] 0 0
Incidence of SAEs
Timepoint [3] 0 0
8 days in SAD part, 17 days for MAD part
Secondary outcome [4] 0 0
Incidence of lab deviations
Timepoint [4] 0 0
8 days in SAD part, 17 days for MAD part

Eligibility
Key inclusion criteria
- 1. Must have given written informed consent 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. Adult males and females, 18 to 65 years of age (inclusive) at screening. 3. Body mass index (BMI) = 18.5 and = 32.0 kg/m2, with a body weight (to 1 decimal place) = 50.0 kg at screening.
Minimum age
18 Years
Maximum age
65 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
* 1. History or presence of significant cardiovascular, pulmonary, hepatic, renal, haematological, gastrointestinal, endocrine, immunologic, dermatologic or neurological disease, including any acute illness or major surgery within the past 3 months determined by the PI to be clinically significant.

2. History of surgery or hospitalisation within 30 days prior to screening, or surgery planned during the study.

3. Acute infections within 4 weeks prior to screening or current infection that requires systemically absorbed antibiotic, antifungal, antiparasitic or antiviral medications.

4. Presence or history of any abnormality or illness, including gastrointestinal surgery, which in the opinion of the PI may affect absorption, distribution, metabolism or elimination of the study drug.

5. Any history of malignant disease in the last 5 years (excludes surgically resected skin squamous cell or basal cell carcinoma).

6. Any screening laboratory result outside the normal laboratory reference range (as confirmed upon repeated testing) and deemed clinically significant by the PI.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Other
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
15/04/2024
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/09/2024
Actual
Sample size
Target
64
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Greater Sydney Are
Recruitment hospital [1] 0 0
Scientia Clinical Research - Sydney
Recruitment postcode(s) [1] 0 0
NSW 2031 - Sydney

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Traws Pharma, Inc.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Ekaterina Dokukina, MD, MPHIL
Address 0 0
Country 0 0
Phone 0 0
+382069728309
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT06402136