MedPath

Health Canada

Health Canada logo
🇨🇦Canada
Ownership
Private, Subsidiary
Established
2010-11-01
Employees
10K
Market Cap
-
Website
http://www.hc-sc.gc.ca

Clinical Trials

4

Active:0
Completed:4

Trial Phases

1 Phases

Not Applicable:3

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (3 trials with phase data)• Click on a phase to view related trials

Not Applicable
3 (100.0%)

Air Pollution, Physical Activity and Cardiovascular Function of Patients With Implanted Cardioverter Defibrillators

Not Applicable
Completed
Conditions
Blood Pressure
First Posted Date
2019-07-18
Last Posted Date
2019-07-18
Lead Sponsor
Health Canada
Target Recruit Count
18
Registration Number
NCT04024852

Commuter Air Pollution Intervention Study

Not Applicable
Completed
Conditions
Cognitive Function
Saliva Stress Hormones
Air Pollution Exposure
Lung Inflammation
Cardiopulmonary Function
First Posted Date
2014-10-28
Last Posted Date
2015-03-02
Lead Sponsor
Health Canada
Target Recruit Count
48
Registration Number
NCT02277002
Locations
🇨🇦

Guy-Favreau Complex, Montreal, Quebec, Canada

News

Iovance Biotherapeutics Implements Major Restructuring Amid Regulatory Setbacks and Commercial Challenges

Iovance Biotherapeutics reduced its workforce by 19% in Q3 2025 and targets $100 million in annual savings to extend cash runway to late 2026.

Iovance Reports Strong Q2 2025 Results with $60M Revenue as Amtagvi Adoption Accelerates

Iovance Biotherapeutics achieved $60.0 million in total product revenue for Q2 2025, representing a 93% year-over-year increase driven by strong Amtagvi adoption.

Rapid Dose Therapeutics Submits QuickStrip Nicotine Oral Film for Health Canada Approval

Rapid Dose Therapeutics has submitted a product application to Health Canada for approval of its QuickStrip Nicotine products in four dose strengths (1-4 mg), marking a significant regulatory milestone for the innovative oral nicotine delivery system.

Health Canada Approves Clearside Biomedical's XIPERE for Uveitic Macular Edema Treatment

Health Canada has granted approval for XIPERE (triamcinolone acetonide injectable suspension) for suprachoroidal use in treating uveitic macular edema, expanding the drug's global reach.

Nanochon Receives Health Canada Approval for First-in-Human Trial of 3D Printed Knee Cartilage Implant

Nanochon has received Health Canada approval for a first-in-human clinical trial of its 3D printed Chondrograft implant to treat articular cartilage defects in the knee.

Health Canada Extends Evkeeza Approval to Infants as Young as 6 Months for Rare Cholesterol Disorder

Health Canada has extended approval of Evkeeza (evinacumab) to treat children as young as 6 months old with homozygous familial hypercholesterolemia (HoFH), a devastating inherited cholesterol disorder.

Solid Biosciences Receives FDA and Health Canada Approval for First-in-Class Gene Therapy Targeting Fatal Heart Rhythm Disorder

Solid Biosciences has received FDA IND and Health Canada CTA approval for SGT-501, a novel gene therapy designed to treat catecholaminergic polymorphic ventricular tachycardia (CPVT), a rare genetic heart condition that can cause sudden death.

MedMira Launches Clinical Trial for Dual HIV/Syphilis Self-Test in Canada

MedMira has launched a clinical trial to evaluate its Multiplo TP/HIV rapid test for self-testing use in Canada, with first participants enrolled at sites in Victoria and Toronto.

AbCellera Advances Two First-in-Class Antibody Therapies to Phase 1 Trials Following Strategic Pivot

AbCellera Biologics has received Health Canada authorization to begin Phase 1 trials for ABCL635, a first-in-class NK3R antagonist targeting menopause-related hot flashes, and ABCL575, an OX40L-targeting antibody for atopic dermatitis, both scheduled to start in Q3 2025.

Quebec Expands Public Reimbursement of Pluvicto Radioligand Therapy for Advanced Prostate Cancer

Quebec implemented public reimbursement of Pluvicto (lutetium-177 vipivotide tetraxetan) as of July 2, 2025, for eligible patients with PSMA-positive metastatic castration-resistant prostate cancer.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.