ethovoaSciences

Pharmaceutical-grade alkaloids, from the source.

Built at the source, not bought on a market.

Ethovoa Sciences is a development-stage pharmaceutical company working toward GMP-qualified supply of ibogaine hydrochloride and its registered starting material, voacangine.

B2B. We supply licensed manufacturers and research institutions only.

A focused programme. A clear chemical pathway. Voacanga africana root bark Voacangine Ibogaine hydrochloride

Our approach

A clear path from source to science.

Ethovoa is developing an integrated model that connects botanical sourcing and upstream processing in Ghana with specialist pharmaceutical development partners. We are building toward a qualified, reproducible supply of voacangine and downstream APIs.

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01 Ghana / Origin

Start at the source.

Work with established Ghana-based relationships to build a traceable supply of Voacanga africana root bark.

Sourcing relationships

02 Ghana / Upstream

Develop the extract.

Develop a consistent voacangine intermediate, with characterisation and quality requirements agreed with our development partners.

Upstream development

03 Global / Collaboration

Build toward GMP.

Engage a qualified Contract Development and Manufacturing Organization to establish the pathway to GMP-grade ibogaine hydrochloride.

Partner discussions

Origin / Ghana, West Africa

Local roots. Global perspective.

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A long-term asset, not a commodity.

We treat the source material as a long-term asset, not a commodity. Our sourcing follows the Nagoya Protocol's access and benefit-sharing framework, with formal engagement through Ghana's national competent authority. The genetic resource itself, not merely the finished extract, is the basis of that commitment.

  • Harvested on a rotational basis to ensure botanical viability
  • Documented origin and formal chain of custody
  • Nagoya Protocol access and benefit-sharing framework
  • Upstream processing located in country, at origin

Our objective is a sourcing and processing framework that supports the rigorous regulatory requirements of future pharmaceutical customers.

Organization

Experience built over years.

Our team combines pharmaceutical chemistry, GMP manufacturing experience and direct in-country relationships across Ghana's growing regions. It was built over years, not assembled for this project.

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Ian MacKenna

Founder, Chief Executive Officer and Lead Chemist

Ian holds a chemistry background from the University of New Orleans and has worked specifically in ibogaine chemistry for approximately three years. He has spent four months in country in Ghana building the sourcing and processing relationships that the programme is founded on.

He is directly responsible for the synthesis pathway, the technical documentation package and engagement with development and manufacturing partners. He speaks and moderates regularly at conferences in the field.

Behind the programme

Ian is supported by a board and operating group whose contributions span the disciplines this programme depends on. We introduce them directly in partner conversations.

  • The originator of the Voacanga total alkaloid extraction methodology, as chairman
  • Supply chain leadership with an established Ghanaian processor network
  • In-country chemistry and facility management, resident in Ghana
  • Corporate structure and business development, from prior company builds
  • Ghana relations, with long-standing community and institutional ties

Our development focus

Voacangine first. A wider horizon.

A focused development programme today, with room to explore the broader potential of Voacanga-derived alkaloids over time.

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01 Voacangine and ibogaine HCl
02 Broader alkaloids
03 Downstream potential

Lead development programme

Primary pipeline

Our initial target is GMP-grade voacangine derived from Ghana-sourced botanical material. We are seeking a qualified CDMO for starting-material assessment, analytical and process development, and a defined chemical pathway toward ibogaine hydrochloride.

Current stage: development and partner evaluation. No commercial GMP supply is being offered at this stage.

Development goals are not statements of regulatory approval or GMP certification. Product specifications, manufacturing scope and availability will be established through the appropriate development and qualification work. Read the full development notice.

Let's start a conversation

The next step starts together.

Have the capabilities, perspective or research needs to help shape this programme? We supply licensed manufacturers and research institutions.

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Direct

General and partnership
info@ethovoa.com
Founder and lead chemist
ian@ethovoa.com

Please do not include confidential technical information or patient data in an initial inquiry.

Let's find common ground

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