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Trial registered on ANZCTR


Registration number
ACTRN12622000293763
Ethics application status
Approved
Date submitted
22/12/2021
Date registered
16/02/2022
Date last updated
11/08/2022
Date data sharing statement initially provided
16/02/2022
Type of registration
Prospectively registered

Titles & IDs
Public title
A study comparing extended release and immediate release formulations of EQ121 in adult healthy volunteers of Chinese descent- Part C
Scientific title
A study comparing the safety, tolerability, and pharmacokinetics of extended release and immediate release formulations of EQ121 in adult healthy volunteers of Chinese descent- Part C
Secondary ID [1] 305972 0
EQ121-010
Universal Trial Number (UTN)
Trial acronym
Linked study record
Part A: ACTRN12622000307707
Part B: ACTRN12622000292774

Health condition
Health condition(s) or problem(s) studied:
Rheumatoid Arthritis 324575 0
Condition category
Condition code
Inflammatory and Immune System 322041 322041 0 0
Rheumatoid arthritis

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
EQ121 immediate release (IR) capsule is an oral solid dosage form manufactured at strengths of 1 mg and 12 mg.
Each EQ121 capsule contains EQ121 drug substance; mannitol, pregelatinized starch and microcrystalline cellulose as diluents; croscarmellose sodium as disintegrant; colloidal silicon dioxide as glidant; and magnesium stearate as lubricant
Part C is a two-sequence, two-period crossover study to compare the oral bioavailability of the EQ121 IR capsule formulation to the EQ121 ER tablet formulation, in adult healthy volunteers of Chinese descent
Sequence 1: In period 1 of Sequence 1, the participants will receive 2 oral doses of 24 mg EQ121 immediate release (IR) capsule given twice a day (e.g. 12 hours apart) on Day 1 under fasting conditions.
Sequence 2: In period 2 of Sequence 2, after completion of Period 1, following a 5-day washout period, the same participants will receive 2 oral doses of 24 mg EQ121 immediate release (IR) capsule given twice a day (e.g. 12 hours apart) on Day 7 under fasting conditions

Five (5) participants will be enrolled into each sequence

Adherence will be monitored via clinical site staff recording and reporting all number of pills taken while confined
Intervention code [1] 322363 0
Treatment: Drugs
Comparator / control treatment
EQ121 extended release (ER) tablet formulation is active group

Sequence 1: In period 2 of Sequence 1, After completion of Period 1, following a 5-day washout period, the same participants will receive a single oral dose of up to 80 mg EQ121 extended release (ER) tablet (dose and formulation to be determined based on data from Part A) on Day 7 under fasting conditions.
Sequence 2: In period 1 of Sequence 2, the participants will receive a single oral dose of up to 80 mg EQ121 extended release (ER) tablet (dose and formulation to be determined based on data from Part A) on Day 1 under fasting conditions.

Each EQ121 tablet contains EQ121 drug substance; lactose monohydrate as diluent; fumaric acid and tartaric acid as acidulant; hydroxypropyl methylcellulose (HPMC) as matrix; colloidal silicon dioxide as glidant; and magnesium stearate as lubricant. Each formulation will be made up of 15% W/W EQ121 drug substance and differing amounts of the excipients listed above

Five (5) participants will be enrolled into each sequence
Adherence will be monitored via clinical site staff recording and reporting all number of pills taken while confined
Control group
Active

Outcomes
Primary outcome [1] 329799 0
To compare the bioavailability of EQ121 immediate-release capsule formulation administered as 2 doses twice a day (BID; 12 hours apart) with a single dose of EQ121 extended release (ER) once daily (QD) tablet formulation in adult healthy volunteers of Chinese descent Blood sample for measurement of plasma EQ121 will be collected
Timepoint [1] 329799 0
Daily from Baseline to Day 12 post dose
Secondary outcome [1] 403880 0
To compare the pharmacokinetics of EQ121 IR capsule formulation between Chinese and non-Chinese healthy volunteers
The following parameter will be used for evaluation of pharmacokinetic
• AUC0-t – area under the concentration-time curve from time 0 to time of last quantifiable concentration(t) calculated using linear trapezoidal rule
• AUC0-inf – area under the concentration -time curve from time 0 to infinity
• AUCextra – area under the concentration -time curve from last quantifiable concentration extrapolated to infinity
• Cmax – maximum observed plasma concentration over the entire sampling during obtained directly from the observed plasma concentration-time data without interpolation
• Tmax – time to reach maximum observed plasma concentration during obtained directly from the observed plasma concentration-time data without interpolation
• Kel – elimination rate constant
• t½ – terminal half-life
• CL/F – apparent clearance
• Vz/F – apparent clearance
Timepoint [1] 403880 0
Blood samples collected at pre-dose and at 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12 (prior to the evening dose), 12.25, 12.5, 13, 13.5, 14, 15, 16, 18, 20, 24, 30, 48 hours and Day 1, 2, 3, 7, 8, 9 post dose
Secondary outcome [2] 403879 0
To evaluate the safety, and tolerability of EQ121 ER tablet formulation following oral single-dose administration in adult healthy volunteers of Chinese descent through adverse events (Severity should be recorded and graded according to the Guidance for Industry Toxicity Grading Scale for Healthy Adult and Adolescent Volunteers Enrolled in Preventive Vaccine Clinical Trials)
Timepoint [2] 403879 0
Once daily from Baseline to Day 12 post dose
Secondary outcome [3] 403878 0
To compare the pharmacokinetics of EQ121 ER tablet formulation between Chinese and non-Chinese healthy volunteers
The following parameter will be used for evaluation of pharmacokinetic
• AUC0-t – area under the concentration-time curve from time 0 to time of last quantifiable concentration(t) calculated using linear trapezoidal rule
• AUC0-inf – area under the concentration -time curve from time 0 to infinity
• AUCextra – area under the concentration -time curve from last quantifiable concentration extrapolated to infinity
• Cmax – maximum observed plasma concentration over the entire sampling during obtained directly from the observed plasma concentration-time data without interpolation
• Tmax – time to reach maximum observed plasma concentration during obtained directly from the observed plasma concentration-time data without interpolation
• Kel – elimination rate constant
• t½ – terminal half-life
• CL/F – apparent clearance
• Vz/F – apparent clearance
Timepoint [3] 403878 0
Blood samples collected at pre-dose and at 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 16, 20, 24, 30, 36, 48, hours and Day 1, 2, 3, 7, 8, 9, 13, 14, 15 and Day 1, 2, 3, 7, 8, 9 post dose

Eligibility
Key inclusion criteria
1. Are capable of giving informed consent and complying with study procedures;
2. Healthy male or female participants, between the ages of 18 and 65 years, inclusive;
3. BMI of 18.0 to 32.0 kg/m2 inclusive and body weight not less than 50 kg;
4. Female participants must not be currently breast-feeding, and must meet one of the following criteria:
a. Surgically sterile for at least 3 months prior to Screening by one of the following means:
• Bilateral tubal ligation
• Bilateral salpingectomy (with or without oophorectomy)
• Surgical hysterectomy
• Bilateral oophorectomy (with or without hysterectomy)
b. Postmenopausal, defined as the following:
• Last menstrual period greater than 12 months prior to Screening without an alternative medical cause,
AND
• Postmenopausal status confirmed by serum FSH concentration at Screening greater than 40 mIU/mL
c. Women of childbearing potential (WOCBP):
• Must not have a positive serum pregnancy test at Screening and must have a negative urine pregnancy test on admission
• Must use at least one of the following protocol-specified highly effective methods of birth control, AND must agree to use barrier contraception (male condom) during heterosexual intercourse, from the time of Screening until at least 30 days after the last dose of study drug:
• Partner vasectomy (at least 6 months prior to Screening; vasectomized partner should be the sole partner of the female participant)
• Combined (estrogen and progestogen containing) hormonal contraception (oral, intravaginal, transdermal, injectable)
• Progestogen-only hormonal contraception (oral, injectable, implantable)
• Implantable device (implantable rod or intrauterine device)
Alternatively, WOCBP must practice complete abstinence (defined as refraining from heterosexual intercourse when this is in line with the preferred and usual lifestyle of the participant; periodic abstinence and withdrawal are not acceptable) from Screening until at least 30 days after the last dose of study drug. It is not necessary to use any other method of contraception when complete abstinence is elected. WOCBP who choose complete abstinence must continue to have pregnancy tests as per protocol. The reliability of sexual abstinence needs to be evaluated by the PI or designee in relation to the duration of the clinical trial and the preferred and usual lifestyle of the participant.
5. Male participants must agree to utilize a highly effective method of contraception (condom) during heterosexual intercourse from clinic admission until 90 days following the last dose of study drug and must refrain from donating sperm for this same period. Vasectomized males do not need to use additional forms of contraception providing that the procedure was performed at least 12 weeks prior to Screening and an absence of sperm in the ejaculate has been documented. Total sexual abstinence may be considered acceptable at the discretion of the PI or designee;
6. Considered healthy by the PI or designee, based on participant’s reported medical history, full physical examination, clinical laboratory tests, 12-lead ECG, and vital signs;
Minimum age
18 Years
Maximum age
65 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
1. Inability to attend all the study visits or comply with study procedures;
2. Evidence or clinically significant history of gastrointestinal, cardiovascular, musculoskeletal, endocrine, hematologic, psychiatric, renal, hepatic, bronchopulmonary, neurologic, immunologic, lipid metabolism disorders, or drug hypersensitivity as determined by the PI or designee;
3. Hospital admission or major surgery within 3 months prior to Screening;
4. A history of drug abuse, or a positive test at Screening or Admission for drugs of abuse;
5. A history of alcohol abuse according to medical history within 6 months prior to Screening (drinking 14units of alcohol per week: 1 unit equal to 360 mL of beer, or 37 mL of spirits, or 120 mL of wine) at Screening or upon admission to the clinical site;
6. Positive screen for drugs of abuse or alcohol at Screening or at Admission;
7. A history of organ transplant, including history of bone marrow transplant;
8. Taken any prescription medications within 14 days or 5 half-lives (whichever is longer), or any injectable prescription medications within 30 days or 10 half-lives (whichever is longer), of the first dose of study drug
9. Taken an investigational drug within 3 months or 5 half-live, whichever is longer, from the Screening date
10. Any liver LFT value greater than 1.5 of ULN which includes aspartate aminotransferase (AST), alanine aminotransferase (ALT), bilirubin, alkaline phosphatase, and gamma-glutamyl transferase (GGT) at Screening or at Admission
11. Any white blood cell (WBC), absolute neutrophil count (ANC), hemoglobin, or platelet count less than the lower limit of normal at Screening or at Admission that is clinically significant in the opinion of the PI or designee
12. Serum creatinine more than upper limit of normal (ULN) at Screening or Admission
13. Any condition or finding that in the opinion of the PI or designee would put the participant or study conduct at risk if the participant were to participate in the study

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
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Crossover
Other design features
Phase
Phase 1
Type of endpoint/s
Safety
Statistical methods / analysis

Recruitment
Recruitment status
Withdrawn
Reason for early stopping/withdrawal
Other reasons/comments
Other reasons
Sponsor has decided not to pursue Sub-study 3 Part C (Chinese Cohort) of Study EQ121-010. This results from a business decision not to evaluate the PK and tolerability of EQ121 specifically in a cohort of exclusively Chinese subjects outside of Mainland China. This decision was not because of any newly identified safety signals or safety risks associated with EQ121.
Date of first participant enrolment
Anticipated
25/07/2022
Actual
Date of last participant enrolment
Anticipated
1/08/2022
Actual
Date of last data collection
Anticipated
12/08/2022
Actual
Sample size
Target
10
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
QLD
Recruitment hospital [1] 21278 0
Q-Pharm Pty - Clive Berghofer Research Centre (CBCRC) - Herston
Recruitment postcode(s) [1] 36147 0
4007 - Herston

Funding & Sponsors
Funding source category [1] 310312 0
Commercial sector/Industry
Name [1] 310312 0
EQRx International, Inc.
Country [1] 310312 0
United States of America
Primary sponsor type
Commercial sector/Industry
Name
EQRx International, Inc.
Address
50 Hampshire Street, Cambridge, MA 02139, USA
Country
United States of America
Secondary sponsor category [1] 311434 0
None
Name [1] 311434 0
Address [1] 311434 0
Country [1] 311434 0
Other collaborator category [1] 282082 0
Commercial sector/Industry
Name [1] 282082 0
Novotech (Australia) Pty Limited
Address [1] 282082 0
Level 3, 235 Pyrmont Street Sydney, NSW Australia - 2009
Country [1] 282082 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 309976 0
Alfred Ethics Committee
Ethics committee address [1] 309976 0
Ethics committee country [1] 309976 0
Australia
Date submitted for ethics approval [1] 309976 0
28/10/2021
Approval date [1] 309976 0
09/11/2021
Ethics approval number [1] 309976 0

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

Contacts
Principal investigator
Name 116046 0
Dr Richard Friend
Address 116046 0
Nucleus Network - Brisbane,
Level 5 Clive Berghofer Cancer Centre Research Centre, 300 Herston Rd, Herston, QLD, 4006, Australia
Country 116046 0
Australia
Phone 116046 0
+61 07 3845 3620
Fax 116046 0
Email 116046 0
r.friend@nucleusnetowrk.com.au
Contact person for public queries
Name 116047 0
Katherine (Kitty) Gunn
Address 116047 0
Nucleus Network Pty Ltd
Level 5, 300 Herston Road, Herston, QLD 4006
Country 116047 0
Australia
Phone 116047 0
+61420611503
Fax 116047 0
Email 116047 0
k.gunn@nucleusnetwork.com.au
Contact person for scientific queries
Name 116048 0
Ramandeep Sharma
Address 116048 0
Novotech (Australia) Pty Limited
Level 3, 235 Pyrmont Street Sydney, NSW, Australia - 2009
Country 116048 0
Australia
Phone 116048 0
+61393411992
Fax 116048 0
Email 116048 0
Ramandeep.Sharma@novotech-cro.com

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided


Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.