Ozmosi | Lidocaine Drug Profile
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Lidocaine

Alternative Names: lidocaine, lignocaine, xylocaine, lidoderm, xylocain, zingo, emla cream, versatis, promescent, lidoderm 5, xylocaine 2%, alphacaine, LIDOCAINA, lidocain, ztlido, akten, glydo, lidopen, anestacon, laryng-o-jet kit, lta ii kit, pediatric lta kit, dentipatch, laryngotracheal anesthesia kit, sx1 medicated post-operative system, lmr plus, lidomark 1/5, lidomark 2/5, lidenzal 1%, lidenzal 2%, prelidopine pre-operative system, lidovix l, venipuncture px1, medicated buccal dna collection kit 2, dermalid, dx1 oragenomic medicated dna collection screen, dx2 oragenomic medicated dna collection screen, medicated buccal dna collection kit, pliaglis, lignospan standard, oraqix, lignospan forte, synera, emla, duocaine, embolex, lidosite topical system kit, iontocaine, lidocaton, octocaine, rocephin kit, lanabiotic, fossaoprin spg2, acunistat-30, acunistat-60, fossaoprin spg4, h-paxin, diclovix, omnitrenidol, lixtraxen 1%, point of care l2, diclovix m, point of care l5, point of care lm 2.2, point of care lm 2.5
Clinical Status: Inactive
Latest Update: 2026-03-03
Latest Update Note: Clinical Trial Update

Product Description

LIDOCAINE (LYE doe kane) is an anesthetic. It causes loss of feeling in the skin and surrounding tissues. It is used to prevent and to treat pain from some procedures. This medicine is also used to treat minor burns, scrapes and insect bites. (Sourced from: https://my.clevelandclinic.org/health/drugs/19854-lidocaine-skin-cream-or-ointment)

Mechanisms of Action: Sodium Channel Blocker

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Intravenous, Topical, Transdermal

FDA Designation: *

Approval Status: Approved

Approved Countries: Algeria | Argentina | Australia | Austria | Bangladesh | Belgium | Bosnia | Brazil | Bulgaria | Canada | Chile | China | Colombia | Croatia | Cyprus | Czech | Denmark | Dominican Republic | Ecuador | Egypt | Estonia | Finland | France | Germany | Greece | Hong Kong | Hungary | Iceland | India | Indonesia | Ireland | Israel | Italy | Japan | Jordan | Korea | Latvia | Lebanon | Lithuania | Luxembourg | Malaysia | Malta | Mexico | Morocco | Netherlands | New Zealand | Norway | Pakistan | Peru | Philippines | Poland | Portugal | Romania | Russia | Saudi Arabia | Serbia | Singapore | Slovakia | Slovenia | South Africa | Spain | Sri Lanka | Sweden | Switzerland | Taiwan | Thailand | Tunisia | Turkey | Ukraine | United Arab Emirates | United Kingdom | United States | Uruguay | Venezuela | Vietnam

Approved Indications: None

Known Adverse Events: None

Company: Endo
Company Location:
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Lidocaine

Countries in Clinic: Australia, Belgium, Canada, China, Czech Republic, France, Germany, Italy, Japan, Netherlands, Norway, Spain, United States

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Anesthesia Related|Cesarean Section|Collagen Diseases|Facial Nerve Diseases|Facial Pain|Injuries/wounds Unspecified|Intervertebral Disc Degeneration|Intestinal Diseases|Low Back Pain|Neuralgia, Postherpetic|Neuropathic Pain|Other|Pain Unspecified|Premature Ejaculation

Phase 2: Abdominal Pain|Anorexia|Chronic Pain|Hearing Loss, Bilateral|Ileus|Pelvic Pain

Phase 1: Diabetic Foot|Idiopathic Pulmonary Fibrosis|Lung Diseases, Interstitial|Progressive Pulmonary Fibrosis|Skin Ulcer

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

CTR20254425

CTR20254425

P1

Completed

Premature Ejaculation

2025-12-15

2026-01-18

NCT05921292

OM-CTP-002

P1

Completed

Skin Ulcer

2024-01-22

2024-06-28

Patient Enrollment|Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT05417425

OM-CTP-003.1

P1

Completed

Diabetic Foot

2023-10-31

2024-06-07

Primary Endpoints

ACTRN12620001141932p

SPPH

P1

Not yet recruiting

Lung Diseases, Interstitial|Idiopathic Pulmonary Fibrosis|Progressive Pulmonary Fibrosis

2021-01-22

NCT07076641

LIDORACHI

P3

Not yet recruiting

Intestinal Diseases

2027-07-30

5%

2025-07-23

Primary Endpoints|Treatments

CTR20212038

CTR20212038

P3

Completed

Neuropathic Pain

2023-11-30

2025-04-29

Patient Enrollment|Primary Completion Date|Start Date|Study Completion Date|Treatments|Trial Status

NCT05088980

NCT05088980

P3

Completed

Other

2023-11-29

10%

2023-12-21

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

2021-006632-67

QETAL

P3

Active, not recruiting

Cesarean Section|Anesthesia Related

2023-09-08

NCT05793892

CU-30101-304

P3

Completed

Collagen Diseases|Facial Nerve Diseases|Facial Pain|Anesthesia Related

2023-08-23

30%

2024-11-13

Primary Completion Date|Primary Endpoints|Start Date|Study Completion Date|Treatments|Trial Status

NCT03737461

RESPINE

P3

Active, not recruiting

Low Back Pain|Intervertebral Disc Degeneration

2022-05-30

27%

2023-08-15

2015-002160-17

2015-002160-17

P3

Active, not recruiting

Pain Unspecified|Injuries/wounds Unspecified

2017-12-24

2022-03-13

Treatments

2023-504466-28-00

SENS-501-101

P2

Recruiting

Hearing Loss, Bilateral

2030-12-31

2025-05-02

Treatments

NCT05923086

ORE001PIIPOI

P2

Recruiting

Ileus

2025-12-31

35%

2024-10-04

Primary Completion Date|Primary Endpoints

NCT05707208

ST-CP-202

P2

Active, not recruiting

Chronic Pain

2025-12-04

2%

2025-12-03

Primary Endpoints

2023-510499-30-00

OREPhIIAnorexia

P2

Not yet recruiting

Anorexia

2025-06-30

2025-05-02

Treatments

2023-508224-35-01

2023-508224-35-01

P2

Recruiting

Abdominal Pain|Chronic Pain

2025-03-31

2025-05-02

Treatments

ACTRN12621000589886

ACTRN12621000589886

P2

Recruiting

Pelvic Pain|Chronic Pain

2023-12-29

2026-02-15

Treatments

ACTRN12625001044415

ACTRN12625001044415

P3

Not yet recruiting

Neuralgia, Postherpetic

2027-09-30

2026-02-15

Treatments

CTR20253835

CTR20253835

P1

Completed

Premature Ejaculation

2025-12-12

2025-12-21

Primary Completion Date|Start Date|Study Completion Date|Treatments|Trial Status

CTR20253834

CTR20253834

P1

Completed

Premature Ejaculation

2025-11-11

2026-01-04

Primary Completion Date|Start Date|Study Completion Date|Treatments|Trial Status

CTR20254137

CTR20254137

P1

Completed

Premature Ejaculation

2025-11-11

2025-12-06

Primary Completion Date

CTR20252515

CTR20252515

P1

Completed

Premature Ejaculation

2025-09-09

2025-10-05

Primary Completion Date|Study Completion Date|Treatments|Trial Status

CTR20252536

CTR20252536

P1

Completed

Premature Ejaculation

2025-08-06

2025-09-07

Primary Completion Date|Study Completion Date|Treatments|Trial Status

2023-507633-21-00

MN45053

P3

Withdrawn

Unknown

2029-07-31

2025-05-02

Treatments

CTR20250271

CTR20250271

P3

Completed

Premature Ejaculation

2025-11-18

2026-01-11