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A double-blind, randomized, placebo-controlled, dose-escalating Phase I trial to determine the safety, pharmacokinetic parameters, and clinical effects of single subcutaneous injections of IGX12 in healthy female and male participants

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-504671-24-00
Acronym
PRO-2022-009
Enrollment
48
Registered
2023-09-15
Start date
2023-09-22
Completion date
2025-07-25
Last updated
2024-08-01

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

Conditions

Men and women infertility

Interventions

None listed

Sponsors

Igyxos
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Countries

Germany

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026