Det foreligger helt klare cash avtaler i Cevira fra Asieris. Det vet du godt. BÄde milestones og royalties % av salg.
- Oslo, Norway, March 3, 2026: Photocure ASA (OSE: PHO), the
Bladder Cancer Company, announces that its partner Asieris Pharmaceuticals (SSE:
- communicated today that its core product APL-1702 (trade name:
CEVIRA[Âź]), has received the Drug Registration Certificate from Chinaâs National
Medical Products Administration (NMPA), enabling commercial launch in China.
Cevira (APL-1702) is a photodynamic drug-device combination product in
development for the non-surgical treatment of high-grade squamous
intraepithelial lesions (HSIL), licensed to Asieris by Photocure. With Ceviraâs
regulatory approval in China, Photocure is eligible for a milestone payment with
further sales milestones based on future revenue.
The announcement from Asieris states: âAs the worldâs first non-surgical, non
-invasive therapy for patients with cervical intraepithelial neoplasia grade 2
(CIN2), APL-1702 is expected to fill a critical clinical gap in this therapeutic
area and redefine a massive, previously underserved market for non-invasive
cervical disease treatment.
In the absence of other approved non-invasive treatment options, APL-1702 has
the potential to reshape a treatment landscape long dominated by surgical and
other invasive or minimally invasive interventions. It will enable a shift from
a âone-size-fits-allâ approach toward one that prioritizes non-invasive therapy,
offering a breakthrough solution to current clinical challenges.â
âThis regulatory milestone is a substantial achievement for a non-surgical
organ-sparing treatment option which addresses an important unmet medical need,â
said Anders Neijber, Photocureâs Chief Medical Officer
Read Asierisâ full media release here: https://asieris.com/asieris-cevira
-approved-in-china-as-first-in-class-non-invasive-therapy-for-cervical
-precancerous-lesions/
@Haltopen kun postet fordi over skaper feilaktig pÄstand at det ikke foreligger avtale om royalties og milestones utbetalinger.
Noen liker Ă„ lage panikk av noe som ikke nĂždvendigvis er det helt store endringer?
Er denne feil ved USA marked :
- Veksten blir det samme som i dag selv om PHO mÄ bruke kun KARL STORZ i USA per dags dato etter FDA avgjÞrelsen fremover