First-in-Human Trial in Healthy Adult Volunteers to Evaluate Safety, Tolerability and PK of LAPIX Study Drug; LPX-TI641

Multiple Sclerosis Clinical Trial

Official title:

A Phase I First in Human, Randomized, Double-blind, Placebo- Controlled Study in Healthy Adult Volunteers to Evaluate Safety, Tolerability and Pharmacokinetics of LPX-TI641 After Single Oral Doses.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05853835
• Other study ID #: LPX641-101
• Status: Recruiting
• Phase: Phase 1
• Start date: October 30, 2023
• Est. completion date: August 1, 2024

Study information

• Verified date: November 2023
• Source: LAPIX Therapeutics Inc.
• Contact: LAPIX Therapeutics Inc.
• Phone: 6172035516
• Email: lpx641-101[@]lapixtherapeutics.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A Phase I First-in-Human, Randomized, Double-Blind, Placebo-Controlled Study in Healthy Adult Volunteers to Evaluate Safety, Tolerability, and Pharmacokinetics after Single Oral Dose of LPX-TI641.

Description:

This is a first-in-human, multi center, randomized, double-blinded, single ascending doses (SAD) Phase I study in healthy adult volunteers (HV). The study will consist of six cohorts (Cohorts 1 to 6) of eight HV subjects administered study drug (LPX-TI641/treatment or placebo oral solution) randomized in a 3:1 ratio (6 treatment + 2 placebo) in each cohort (Total 48 HV). Additional cohorts may be enrolled if deemed appropriate by the Sponsor to repeat a dose level or study another dose level based on the observed safety and PK data from the previous cohorts. Each entire cohort of 8 HV subjects will be enrolled at the same site.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 48
• Est. completion date: August 1, 2024
• Est. primary completion date: April 15, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria: Healthy volunteers

1. Subject has signed an Informed Consent Form (ICF) prior to any study-specific procedures being performed

2. Healthy volunteers (HV) with no known acute or chronic medical conditions (respiratory, gastrointestinal, renal, hepatic, hematological, lymphatic, neurological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, dermatological, endocrine, etc.) at the time of enrollment.

3. All male and non-pregnant females aged 18-55 years old irrespective of their race and ethnicity.

4. Body Mass Index (BMI) 18.0-30.0 kg/m2, inclusive at screening.

5. Clinical laboratory evaluations performed at screening, are within acceptable normal reference ranges (Grade 1 abnormalities may be acceptable if deemed necessary by the investigator. Grade 2 or higher would be exclusionary).

6. Subjects who are willing and able to adhere to study protocol requirements including but not limited to scheduled outpatient visits, inpatient hospital stay, laboratory tests, and 12-lead ECG.

7. Contraception - All subjects (male and female) must agree to use any two of the highly effective contraception methods listed below. This criterion must be followed from the time of the first dose of study medication for 6 weeks after the last dose in females and for 90 days after the last dose for males. a. The following applies to all female volunteers with childbearing potential and female partners of male volunteers enrolled in the study. i. Implantable progestogen-only hormone contraception associated with inhibition of ovulation. ii. Intrauterine device. iii. Intrauterine hormone-releasing system. iv. Bilateral tubal occlusion. v. Combined (estrogen- and progestogen-containing) hormonal contraception associated with inhibition of ovulation: 1) Oral 2) Intravaginal 3)Transdermal 4) Injectable vi. Progestogen-only hormone contraception (oral or injectable) is associated with inhibition of ovulation. vii. Vasectomized partner viii. Sexual abstinence -this is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study intervention. The reliability of sexual abstinence needs to be evaluated about the duration of the study and the preferred and usual lifestyle of the participant. b. The following applies to all male subjects in the study: i. Sexual abstinence- this is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study intervention. The reliability of sexual abstinence needs to be evaluated for the duration of the study and the preferred and usual lifestyle of the participant. ii. A combination of male condoms with either cervical cap, diaphragm, or sponge with spermicide (double-barrier methods). iii. Vasectomy Exclusion Criteria: Healthy volunteers

1. Any known history of malignancy

2. Any known history of asthma

3. COVID-19:

The subject has COVID-19 positive status (confirmed by clinical signs and symptoms and a positive SARS-CoV-2 NAAT result COVID test) at any time during the screening period. OR has had recent COVID-19 vaccination including a booster dose in the past 30 days OR has received anti-viral therapy intended to prevent COVID-19 such as nelmetavir/ritonavir, remdesivir, molnupiravir, interferons, Anti-SARS-CoV-2 monoclonal antibodies, IVIG SARS-CoV-2, COVID-19 Convalescent plasma, etc. within the past 30 days

4. Subject with positive results for HBsAg (hepatitis B surface antigens) and/or HBcAb (Hepatitis B core antibodies) and/or HCV Ab (hepatitis C antibodies), and/or HIV Ab (human immunodeficiency virus antibodies).

5. Blood loss of >250 mL or donated blood within 56 days or donated plasma within 7 days of screening.

6. Recent vaccination with live attenuated vaccines such as influenza, MMR, Herpes zoster, varicella, yellow fever, Rotavirus vaccine, etc., or inactivated vaccines such as Hepatitis A, Rabies vaccine, etc. in the past 30 days.

7. Abnormal amylase levels (Grade 2 or greater)

8. Clinically significant ECG abnormalities (QTcF >450 ms for males and QTcF >470 ms for females).

9. History of or current compulsive abuse of alcohol or positive test for alcohol at screening or Day 0 of Visit 1

10. History of or current use of or positive test at screening or Day 0 of Visit 1 for drugs such as marijuana, cocaine, phencyclidine [PCP], crack, opioid derivatives including heroin, and amphetamine derivatives.

11. Consumption of any beverages or food containing alcohol or drugs such as marijuana, cocaine, phencyclidine [PCP], crack, opioid derivatives including heroin, and amphetamine derivatives from screening until donating the last sample of the study

12. Use of medications for the timeframes specified below, except for medications exempted by the Investigator on a case-by-case basis because they are judged unlikely to affect the PK profile of the study drug or subject safety (e.g., topical drug products

without significant systemic absorption):

• prescription medications within 14 days prior to dosing or 5 half-lives, whichever is longer;
• over-the-counter products and natural health products (including herbal remedies homeopathic and traditional medicines, probiotics, food supplements such as vitamins, minerals, amino acids, essential fatty acids, and protein supplements used in sports) within 14 days prior to dosing or 5 half-lives, whichever is longer, except for the occasional use of paracetamol (up to 2 g daily);
• any prescription or over-the-counter medication or natural health products used for the treatment of irregular bowel transit (e.g,. diarrhea, constipation) within 4 weeks prior to dosing;
• depot injection or implant of any drug within 3 months prior to dosing;
• use of any drugs known to induce or inhibit hepatic metabolism (including St. John's Wort [hypericin]) within 14 days prior to dosing.

13. The subject has participated in another investigational study involving any investigational product within 60 days, or 5 half-lives, whichever is longer, before the dose of the study drug.

14. Pregnant or lactating women or women currently undergoing infertility treatments or women who intend to become pregnant during the time of study enrollment.

15. Involvement in the planning and conduct of the study (applies to CRO staff or staff at the study site).

Related Conditions & MeSH terms

• Autoimmune Diseases
• Multiple Sclerosis

Intervention

Drug:
• LPX-TI641
LAPIX Therapeutics Inc (LAPIX) has developed LPX-TI641, a small molecule for immune tolerance restoration/induction that is an orally bioavailable Tim family agonist (Tim-3 and Tim-4).

Locations

Country	Name	City	State
Jordan	Triumpharma clinical research unit at Alessra Hospital	Amman
United States	AXIS Clinicals	Dilworth	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
LAPIX Therapeutics Inc.

Countries where clinical trial is conducted

United States,  Jordan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To evaluate the safety and tolerability after single ascending oral doses of LPX-TI641 in healthy adult volunteers.	Proportion of subjects with AEs, SAEs and DLTs will be recorded.	14 days
Secondary	To evaluate (Cmax)	To evaluate the Maximum observed plasma concentration (Cmax),after single ascending oral doses of LPX-TI641 in healthy adult volunteers	1 day
Secondary	To evaluate tmax	To evaluate the time to first occurrence of Cmax (tmax), after single ascending oral doses of LPX-TI641 in healthy adult volunteers.	1 day
Secondary	To evaluate AUC0-last	To evaluate Area under the plasma concentration-time curve from time 0 to the time last concentration measurement (AUC0-last) after single ascending oral doses of LPX-TI641 in healthy adult volunteers.	1 day
Secondary	To evaluate AUC0-24	To evaluate Area under the plasma concentration-time curve from time 0 to 24 hr (AUC0-24)after single ascending oral doses of LPX-TI641 in healthy adult volunteers.	1 day
Secondary	To evaluate AUC0-8	To evaluate area under the plasma concentration-time curve from time 0 to infinity (AUC0-8), after single ascending oral dose of LPX-TI641 in healthy adult volunteers.	1 day
Secondary	To evaluate %AUCextrap	To evaluate percentage AUC extrapolated (%AUCextrap) after single ascending oral doses of LPX-TI641 in healthy adult volunteers.	1 day
Secondary	To evaluate t1/2z	To evaluate terminal disposition phase half-life (t1/2z), after single ascending oral doses of LPX-TI641 in healthy adult volunteers.	1 day
Secondary	To evaluate Vz/F	To evaluate apparent volume of distribution during the terminal phase after extravascular administration (Vz/F) after single ascending oral doses of LPX-TI641 in healthy adult volunteers.	1 day
Secondary	To evaluate CL/F	To evaluate apparent clearance after extravascular administration (CL/F), after single ascending oral doses of LPX-TI641 in healthy adult volunteers.	1 day