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Full pipeline overview

All programmes are investigational. Not approved for any indication.

Programme DiscoveryPreclinicalIND / CE-enablingClinical / Launch
PLA-REGEN Regenerative
PLA-CHEMO-1 Oncology
PLA-ONCO-1 Oncology
PLA-ONCO-2 Oncology
Regenerative Oncology All programmes are investigational. Not approved for any indication.

Programme by programme

PLA-REGEN

Regenerative
Indication
Regenerative medicine (aesthetic, orthopaedics, ophthalmology, wound care)
Payload
RNA-enriched platelet preparation (enhanced PRP / hPL kit)
Regulatory route
Under definition (EU)
Notes
Regulatory classification under definition with the competent authorities. Not yet CE-marked. Lead indication: aesthetic (cash-pay).

Stage progression

Discovery 100%
Preclinical
IND / CE-enabling
Clinical / Launch

PLA-CHEMO-1

Oncology
Indication
Solid tumours (lead: pancreatic cancer)
Payload
Gemcitabine
Regulatory route
ATMP / Hospital Exemption (EU) · IND / 505(b)(2) (US)
Notes
Entering preclinical. 505(b)(2) regulatory optionality (US).

Stage progression

Discovery 100%
Preclinical 8%
IND / CE-enabling
Clinical / Launch

PLA-ONCO-1

Oncology
Indication
Pancreatic ductal adenocarcinoma (PDAC)
Payload
siRNA vs KRAS G12D
Regulatory route
ATMP / Hospital Exemption (EU) · IND (US)
Notes
Entering preclinical. First-in-class genetic payload via PTT.

Stage progression

Discovery 100%
Preclinical 8%
IND / CE-enabling
Clinical / Launch

PLA-ONCO-2

Oncology
Indication
Solid tumours (to be determined)
Payload
Genetic payload (TBD)
Regulatory route
TBD
Notes
Discovery-stage programme. Payload and indication under evaluation.

Stage progression

Discovery 45%
Preclinical
IND / CE-enabling
Clinical / Launch

Regulatory & forward-looking statement notice

All Plasfer programmes are investigational and have not been approved by any regulatory authority. PLA-REGEN's regulatory classification is being defined with the competent authorities and it is not yet CE-marked. PLA-CHEMO-1 and PLA-ONCO-1 are in preclinical development; no IND or CTA has been filed. Programme timelines and regulatory routes are subject to change. No claims of safety or efficacy are made. This content may contain forward-looking statements; actual results may differ materially.

Interested in co-developing a PTT programme?

We are open to scientific collaboration, licensing discussions, and co-development agreements for payload classes and indications outside Plasfer's current portfolio.