
NANEXA: Clinical milestones align ahead of phase Ib/II and licensing push
Nanexa continues to strengthen the foundation for the upcoming Phase Ib/II study in the NEX-22 project, with preliminary PK data
NANEXA
Nanexa is a drug delivery company with an in-house developed and patented drug delivery platform, PharmaShell®, which is used for the formulation of injectable depot drugs that create a supply of drugs to the blood. The PharmaShell process is based on ALD (Atomic Layer Deposition) technology, which encloses pharmaceutical particles with a thin shell and creates the opportunity for pharmaceutical companies to develop completely new pharmaceutical products. Nanexa currently collaborates with several pharmaceutical companies.
ANALYSER

Nanexa continues to strengthen the foundation for the upcoming Phase Ib/II study in the NEX-22 project, with preliminary PK data

Nanexa’s Q4 report did not reveal much new, although the conference call provided welcome clarity on the rationale behind the

After initiating dosing of the first patient in June with Nanexa’s long-acting depot formulation of the GLP-1 analog liraglutide, NEX-22

Apart from a slight further delay in the start of Phase I with NEX-22, the report for Q1’24 proved rather

Apart from a write down of capitalized development related to the suspended projects NEX-18 and NEX-20, there was not much

Following the focusing of the roadmap after the rights issue in October, Nanexa has now announced a further streamlining of

With the dust settling after the recent rights issue, Nanexa now progresses with its more focused roadmap, concentrating on Phase

With a subscription rate of 34.7% of the rights issue, and a utilization of guarantee commitments corresponding to 27.1%, Nanexa

With the recently completed Phase 1 study for NEX-20 yielding positive results, and the widespread global interest in GLP-1, Nanexa

As we had expected, Nanexa announced a SEK 121m rights issue, albeit at a slightly higher than expected both discount

Nanexa’s Q2’23 advancements with NEX-20 and NEX-22 underscore the company’s forward momentum. NEX-20 is set to provide a more detailed

After positive pre-clinical results in rats with NEX-22 (for treatment of type 2 diabetes) in Q1, we now see results

After a news packed Q4 2022, including an exclusivity and evaluation agreement with Novo Nordisk, start of Phase I with

The combination of an exclusive evaluation agreement and directed share issue to Novo Nordisk, global leader in diabetes treatment, provides

Besides starting its third proprietary development project in Q2 (NEX-22, a long-acting formulation of liraglutide for treatment of type 2

Nanexa’s next proprietary development project, NEX-22, is a long-acting formulation of liraglutide for treatment of type 2 diabetes (T2D). Addressing

Johan Widmark | 2022-06-13 08:00 READ FULL REPORT HERE IN PDF New facility up and running While the inauguration of

Med en plan framåt för NEX-18 och nya produktionsanläggningen snart i drift ser vi ljust på chanserna för ett avtal

Efter att Nanexa funnit en lösning och väg framåt med den pausade fas I-studien med NEX-18 står det samtidigt klart

Efter måttliga hudreaktioner på injektionsstället har Nanexa pausat fas I-studien med NEX-18 i väntan på utredning, samtidigt som studien redan
ABOUT NANEXA
CEO: David Westberg
TICKER: NANEXA
LIST: First North
WEB: https://nanexa.com/
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