Skip to content

An Open Label Balanced Randomized Single Dose Two Treatment Two Sequence Two Period Two Way Crossover Oral Bioavailability Study Comparing Apixaban 5 mg Oral Solution 1mg/mL Manufactured by XL Laboratories Pvt Ltd 430 DLF Towers Shivaji Marg New Delhi India

An Open Label Balanced Randomized Single Dose Two Treatment Two Sequence Two Period Two Way Crossover Oral Bioavailability Study Comparing Apixaban 5 Mg Oral Solution 1mg Per Ml Manufactured By Xl Laboratories Pvt Ltd 430 Dlf Towers Shivaji Marg New Delhi 110015 India With Eliquis Apixaban 5 Mg Film Coated Tablets Marketing Authorisation Holder Bristol Myers Squibb Pfizer Eeig Plaza 254 Blanchardstown Corporate Park 2 Dublin 15 D15 T867 Ireland In Healthy Adult Human Subjects Under Fasting Conditions - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074038
Enrollment
28
Registered
2024-09-19
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Apixaban 5 mg Oral Solution (1mg/ml): Apixaban 5 mg Oral Solution 1 mg/ml single dose oral administration Control Intervention1: Eliquis (Apixaban) 5 mg Film Coated Tablets: Eliquis (Ap

Sponsors

Mahashiv Limited
Lead Sponsor
SpinoS Lifescience And Research Private Limited
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Normal healthy adult human subjects of age between 18 to 45 years and Body Mass Index BMI ranges between 18.50 kg/m2 to 30.00 kg/m2 Subjects who have no evidence of underlying disease during screening and check in and whose screening is performed within 21 days of check in Subjects whose screening laboratory values are within normal limits or considered by the physician or principal clinical investigator to be of no clinical significance Healthy as documented by the medical history physical examination including but may not be limited to an evaluation of the cardiovascular gastrointestinal respiratory musculoskeletal and central nervous system and vital sign assessments Generally healthy as documented by 12-lead electrocardiogram ECG Chest X- Ray and clinical laboratory assessments Willing to consume Ovo lacto-vegetarian diet Willing to comply to all requirements of this study protocol as well as instructed by the study personnel Non smokers Generally healthy as documented by gynaecological examination and breast examination

Exclusion criteria

Exclusion criteria: Evidence of allergy or known hypersensitivity to Apixaban or its inactive ingredients Subjects with hepatic encephalopathy cholestasis myasthenia pre existing liver disease alcohol abuse existing tinnitus and pre existing gallbladder disease Any major illness in the last three months or any significant ongoing chronic medical illness Renal or liver impairment History of alcohol addiction or abuse Consumption of caffeine and or Xanthine containing products coffee tea chocolate and caffeine containing sodas cola etc cigarettes and tobacco containing products for at least 48.00 hours prior to check-in and throughout the entire study Consumption of alcohol and its products grapefruit and or its juice and poppy containing foods within 48.00 hours prior to clinic admission and throughout the entire study Subjects who have taken any prescription medications within 14 days prior to study check in and throughout the study and any over the counter medicinal products herbal medications within 07 days prior to study check in and throughout the study Subjects who have taken an unusual diet for whatever reason for 48.00 hours prior to dosing and throughout the study Subject who had participated in any other study within the 90 days of check in History of difficulty in swallowing History of difficulty in accessibility of veins Positive results for urine screen of drugs of abuse Marijuana THC amphetamine AMP barbiturates BAR cocaine COC benzodiazepines-BZD and morphine MOR in urine prior to check-in of this study period Any blood donation excess blood loss within 90 days of check in Ingestion of any hormonal agent at any time within 14 days prior to start of study check in Use of hormone replacement therapy for a Period of 06 months prior to dosing

Design outcomes

Primary

MeasureTime frame
To assess the Bioavailability on Apixaban 5 mg Oral Solution 1mg/mL Manufactured by XL Laboratories Pvt Ltd 430 DLF Towers Shivaji Marg New Delhi 110015 India With Eliquis Apixaban 5 mg Film Coated Tablets Marketing Authorisation Holder Bristol Myers Squibb Pfizer EEIG Plaza 254 Blanchardstown Corporate Park 2 Dublin 15 D15 T867 Ireland In Healthy Adult Human Subjects Under Fasting ConditionsTimepoint: 23 blood samples 00.00 hrs 00.25 hrs 00.50 hrs 00.75 hrs 01.00 hrs 01.33 hrs 01.67nhrs 02.00 hrs 02.33 hrs 02.67 hrs 03.00 hrs 03.33 hrs 03.67 hrs 04.00 hrs 04.50 hrs 05.00 hrs 06.00 hrs 08.00 hrs 12.00 hrs 24.00 hrs 36.00 hrs 48.00 hrs and 72.00 hrs

Secondary

MeasureTime frame
To monitor the safety and tolerability of single dose administered in healthy adult human subjects under fasting conditionsTimepoint: 23 blood samples 00.00 hrs 00.25 hrs 00.50 hrs 00.75 hrs 01.00 hrs 01.33 hrs 01.67nhrs 02.00 hrs 02.33 hrs 02.67 hrs 03.00 hrs 03.33 hrs 03.67 hrs 04.00 hrs 04.50 hrs 05.00 hrs 06.00 hrs 08.00 hrs 12.00 hrs 24.00 hrs 36.00 hrs 48.00 hrs and 72.00 hrs

Countries

India

Contacts

Public ContactDr Pradeep T

Spino Life science and research private limited

pradeep.t@spinoslifescience.com8220586899

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026