Ozmosi | LB-03002 Drug Profile
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LB-03002

Alternative Names: lb-03002, lb03002, lb 03002
Clinical Status: Inactive
Latest Update: 2012-10-05
Latest Update Note: Clinical Trial Update

Product Description

LB03002 is a novel, sustained-release recombinant human GH, developed for once-a-week s.c. injection. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/19074465/)

Mechanisms of Action: GHR Agonist

Novel Mechanism: No

Modality: Coagulation Factor

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: BioPartners
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Deficiency Diseases|Pituitary Diseases|Dwarfism, Pituitary|Hypopituitarism|Other

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

2005-000346-36

2005-000346-36

P3

Completed

Other

None

2025-07-02

2006-002278-24

2006-002278-24

P3

Completed

Hypopituitarism

2008-09-05

2025-07-02

Treatments

NCT00596037

BPLG-005-RO

P3

Completed

Pituitary Diseases|Deficiency Diseases|Hypopituitarism|Dwarfism, Pituitary

2008-09-01

2019-03-18

Treatments

2005-000384-26

2005-000384-26

P3

Completed

Hypopituitarism

2008-03-04

2022-03-12

Treatments

Recent News Events

Date

Type

Title