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Ireland· IE-PA-EU/1/25/1996/001

Waskyra 2-10 × 106 cells/mL dispersion for infusion

A other hematological agents product containing autologous cd34+ haematopoietic stem cells transduced ex vivo with a lentiviral vector encoding human wiskott-aldrich syndrome protein, registered in Ireland by Fondazione Telethon Ets. The same ATC class is registered in 4 of our 19 countries.

ATC B06

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedWaskyra 2-10 × 106 cells/mL dispersio…ATCB06REGISTER NO.IE-PA-EU/1/25/1996/001PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Autologous cd34+ haematopoietic stem cells transduced ex vivo with a lentiviral vector encoding human wiskott-aldrich syndrome protein is registered in 4 of 19 countries.

Countries holding a registration under ATC B06 (other hematological agents), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 1 of them publish a price we can compare per daily dose

Autologous cd34+ haematopoietic stem cells transduced ex vivo with a lentiviral vector encoding human wiskott-aldrich syndrome protein · ATC B06

4 / 19 countries

  • Denmark
  • Finlandprice
  • Ireland
  • Netherlands
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

HPRA (Ireland)
Active substance
Autologous CD34+ haematopoietic stem cells transduced ex vivo with a lentiviral vector encoding human Wiskott-Aldrich syndrome protein
Manufacturer
Fondazione Telethon Ets
Country
Ireland (IE)
ATC code
B06
ATC class
OTHER HEMATOLOGICAL AGENTS
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/25/1996/001

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of HPRA (Ireland). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/af678a65-869d-4b9d-b278-89ab3a3b8ac6
GET /v1/drugs/af678a65-869d-4b9d-b278-89ab3a3b8ac6?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "form": "Dispersion for infusion",
  "routes": [
    "Intravenous use"
  ],
  "source": "hpra",
  "atc_all": [
    "B06"
  ],
  "strength": null,
  "pa_number": "EU/1/25/1996/001",
  "substances": [
    "Autologous CD34+ haematopoietic stem cells transduced ex vivo with a lentiviral vector encoding human Wiskott-Aldrich syndrome protein"
  ],
  "legal_basis": "Known active substance (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "09/01/2026",
  "dispensing_status": "Product subject to prescription which may not be renewed (A)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

See everything about autologous cd34+ haematopoietic stem cells transduced ex vivo with a lentiviral vector encoding human wiskott-aldrich syndrome protein.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.