Portrait of Levana Sani
Photo: Courtesy of NalaGenetics · Publisher-directed editorial display; source copyright retained

FigureAsia 35 Under 35 · Healthcare

Levana Sani

Age 33 · Pharmacogenomics and precision medicine · Singapore and Jakarta

Founder behind a pharmacogenomics programme spanning real-world outpatient feasibility and a 1,500-patient precision-prescribing initiative.

Approximate age at 31 December 2025
33
Field
Healthcare
Country or region
Singapore and Jakarta
FigureAsia U35 Assessment
90.0 / 100

Career and documented record

Levana Sani has spent years addressing an imbalance in precision medicine: drug-response evidence and commercial tests have been shaped disproportionately by populations outside Southeast Asia. In 2025, a real-world outpatient feasibility study examined how pharmacogenomic testing could be introduced into clinical workflows, documenting practical questions around sampling, interpretation and clinician use rather than treating a genetic report as a self-executing intervention.

Her company also advanced PRECISE-CIP, a programme designed around 1,500 patients and the use of genetic information to guide medication choice. The work sits between laboratory testing, software interpretation and the realities of prescribing in Asian health systems. Sani's personal agency is unusually direct: trained as a scientist, she cofounded the company, led its market and evidence strategy, and has sustained a public partnership with Indonesia's health authorities around genomic capacity.

The programme should not be read as proof that every tested patient experienced a better outcome. Public evidence is stronger on feasibility, implementation and cohort building than on randomized clinical benefit. Its importance lies in creating an Asia-specific evidence base and care pathway where none can be assumed from Western datasets.

Why Levana Sani is on the list

FigureAsia selected Sani because she has joined population representation to clinical implementation. The 2025–2026 record moves pharmacogenomics from a scientific argument into outpatient workflow and a sizeable regional programme. Her score rewards access, agency and Asian significance; it remains conservative on impact because clinical outcome and cost-effectiveness evidence is still developing.

The 2025–26 record

Principal milestone

1,500-patient precision-prescribing programme

Evidence record

Peer-reviewed 2025 outpatient feasibility study

Scale or implementation

Formal genomic-development collaboration with Indonesia's health ministry

The work in its field

Within pharmacogenomics and precision medicine, the relevant test is whether a result can survive scrutiny of maturity, attribution, validity and practical fit. That distinction matters: completed evidence is not projected benefit, and individual responsibility is not interchangeable with the wider team’s achievement.

Assessment breakdown

90.0out of 100

01

Substantive 2025–2026 contribution

18 / 20

The score reflects completed 2025–26 work in pharmacogenomics and precision medicine, assessed at the documented maturity of clinical implementation and cohort development.

02

Verified impact

13.5 / 15

Impact credit is limited to the measured study, regulatory, implementation or operating record stated in the profile; unsupported patient benefit is excluded.

03

Originality and distinction

8 / 10

The work creates or materially advances a distinctive capability within pharmacogenomics and precision medicine rather than relying on title or institutional association.

04

Field and industry influence

8 / 10

The assessment recognises demonstrated effects on research, product development, care delivery or professional practice, with publicity alone carrying no weight.

05

Individual agency

10 / 10

Named authorship and the documented role of Cofounder and Chief Executive Officer establish individual responsibility while preserving credit for collaborators.

06

Durability and trajectory

4.5 / 5

The cited work forms part of a continuing programme, platform or research trajectory rather than a single uncompleted announcement.

07

Asian significance and global relevance

5 / 5

The Asian connection is material to the person's identity, operating base or populations served: Indonesian scientist and founder building pharmacogenomics infrastructure in Southeast Asia.

08

Clinical and scientific validity

6.3 / 7

Clinical and scientific validity is calibrated to clinical implementation and cohort development, with the profile retaining the evidence boundary attached to the result.

09

Safety, quality and responsible governance

6.3 / 7

Safety and governance credit reflects accurate regulatory language, study limitations, data stewardship and the refusal to turn early evidence into clinical certainty.

10

Translation and care-pathway fit

5.4 / 6

The work is scored for its demonstrated fit with a laboratory, regulatory, clinical, operational or public-health pathway, not for projected future adoption.

11

Access, equity and resource stewardship

5 / 5

Access credit reflects documented reach, capacity, affordability or inclusion while distinguishing service volume from proven clinical outcome.

Evidence and attribution

Material claims on this page are supported by the edition’s evidence record. FigureAsia tests age, identity, role, result and individual attribution before publication. Public profiles present the reported record; supporting documentation is retained for accuracy review and corrections.

Achievement records
4
Assessment window
2025–26
Editorial status
Included in the 2026 FigureAsia 35 Under 35 edition

Rights and credit

The portrait is published under the rights basis recorded for this edition. Third-party ownership and reuse restrictions remain in force.

Publication status
Published under a documented rights basis
Credit
Courtesy of NalaGenetics
Licence
Publisher-directed editorial display; source copyright retained
Portrait source and credit