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Developmental Phase

  • Phase I

  • Phase I/II

  • Phase II

  • Phase II/III

  • Phase III

  • Phase IV

  • Others

Trial Status

  • Not yet recruiting

  • Active

  • Completed

Recruitment Status

  • Not yet recruiting

  • Recruiting

  • Completed

  • Terminated

  • Stop recruiting

  • Suspended

  • Study ended

Trial scale

  • Multi-Regional Multi-Center

  • Taiwan Multiple Center

  • Taiwan Single Center

The expected start time interval of the test

-

Trial Applicant

  • Hospital/Foundation

  • Pharmaceutical/Biopharmaceutical company

  • Contract Research Organization

Important Roles

  • Asia Regional PI

  • Taiwan National PI

  • Chairman/Global PI

  • Steering Committee

  • Advisory board

  • None

Audit by Sponsors/CRO

  • Sponsors

  • CRO

  • None

Investigator-initiated trial(IIT)

  • Yes

Filters

Study Statistics

5316Cases

20022027

Total

5316

  • I

    573

  • I/II

    251

  • II

    1225

  • II/III

    138

  • III

    2607

  • IV

    105

  • Others

    356

Principal Investigator

2769Doctors

Co-Principal Investigator

8934Doctors

Hospital

125Sites

List

5316Cases

2026-05-11 - 2030-01-07

Phase III

Not yet recruiting
Efficacy and safety of NNC0487-0111 compared to placebo on morbidity and mortality in people with heart failure with preserved or mildly reduced ejection fraction and obesity (HF-POLARIS).

  • Condition/Disease

    Heart Failure, Obesity

  • Test Drug

    NNC0487-0111 B

Participate Sites
5Sites

Not yet recruiting5Sites

2025-01-03 - 2028-12-31

Phase III

Active
MAGNITUDE-2: A phase 3, multinational, randomized, double-blind, placebo-controlled trial evaluating the efficacy and safety of NTLA-2001 in participants with transthyretin amyloid disease (ATTRv-PN), a hereditary polyneuropathy.

  • Condition/Disease

    Transthyretinopathy with hereditary polyneuropathy (ATTRv-PN)

  • Test Drug

    NTLA-2001

Participate Sites
3Sites

Recruiting3Sites

2025-01-06 - 2027-01-04

Phase I

Not yet recruiting
A phase Ib/IIa, open-label, dose-escalation and dose-expansion trial was conducted in patients with advanced or metastatic colorectal cancer to evaluate the safety, tolerability, and preliminary efficacy of HCB101, cetuximab/bevacizumab, and FOLFOX/FOLFIRI in combination.

  • Condition/Disease

    Advanced or metastatic rectal cancer

  • Test Drug

    HCB101

Participate Sites
1Sites

Recruiting1Sites

2025-02-01 - 2029-02-01

Phase IV

Active
A prospective, observational trial to evaluate the safety and efficacy of copper sulfate® capsules in treating patients with Wilson's disease.

  • Condition/Disease

    Wilson's disease

  • Test Drug

    MetaCu® Capsules 300mg

Participate Sites
2Sites

Recruiting2Sites

2025-03-01 - 2028-09-01

Phase III

Active
A randomized, double-blind, double-dummy, placebo-controlled, multicenter phase 3 trial was conducted in adult and adolescent patients with moderate to severe hidradenitis suppurativa to evaluate the efficacy, safety, and tolerability of two doses of remibrutinib for 68 weeks (RECHARGE-1).

  • Condition/Disease

    suppurative hidradenitis

  • Test Drug

    LOU064

Participate Sites
3Sites

Recruiting3Sites

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