Vetbiolix
Products

Pipeline

Vetbiolix has built an innovative clinical-stage pipeline of 3 First-in -class assets, currently in clinical-stage in Human, acquired through exclusive & Worldwide Licensing deals with Human Biotech Companies.

VBX-2000 (ADENOSINE-A3 AGONIST) - Osteoarthritis

VBX-2400 Canine Osteoarthritis

Preclinical ( Réalisée)
Clinical POC ( Réalisée)
Pilot Study - Placebo Ctrl ( Non réalisée)

VBX-2300 Feline Osteoarthritis

Preclinical ( Réalisée)
In preparation ( Non réalisée)

VBX-1000 (CATHEPSIN-K INHIBITOR) - Periodontitis

VBX-1200 Canine Periodontitis

Preclinical ( Réalisée)
Clinical POC ( Réalisée)
Pilot Study - Placebo Ctrl ( Non réalisée)

VBX-1100 Feline Periodontitis

Preclinical ( Réalisée)
Clinical POC ( Réalisée)
In preparation ( Non réalisée)

VBX-3000 (5HT-4 AGONIST) - Gut Motility Disorders

VBX-3500 Feline coprostasis & megacolon

Preclinical ( Réalisée)
Clinical POC ( Non réalisée)

VBX-3600 Canine GI motility disorders

Preclinical ( Réalisée)
Clinical POC ( Non réalisée)

NEW ASSET

Thanks to a validated track-record on licensing-in operation since Vetbiolix inception, we are actively seeking new opportunities for innovative assets currently in development for Human to develop them for Pets.

6

On-going programs with 3 assets for both Dogs & Cats

Clinical

Stage of development from all Vetbiolix assets

3

Clinical POC studies positive to date

2

On-going Clinical Pilot studies (randomized, placebo-control, double-blind, dose-ranging, EU multicentric)

VBX-2000

VBX-2000 is a patented, First-in-class, oral small molecule, Adenosine-A3 Agonist treating cartilage degradation and reducing inflammation. This product is developed to answer to the crucial unmet medical need to treat the cause of Osteoarthritis (OA), i.e. cartilage degradation and inflammatory process.

Vetbiolix launched in 2024 a proof-of-concept (PoC) clinical study assessing the efficacy and safety of VBX-2000 in client-owned dogs with spontaneously developed OA. The results provide initial evidence of the efficacy of twice-a-day oral administration of VBX-2000 for 90 days against major clinical manifestations of OA. They provide the first proof of clinical effectiveness of a new therapeutic class for better management of osteoarthritis in dogs. With the safety profile observed throughout the treatment period, these results support further development of VBX-2000 in this indication. VBX-2000 is currently assessed in a regulatory, multricentric (Europe), randomized, double-blind, placebo-control, dose-ranging Pilot Clinical Study with Top-line results expected by Q3-2026.

Dogs suffering from OA from 1 to 7 years of age
0 %
Cats suffering from OA from 4 to 11 years of age
0 %
annual global OA therapeutic market in 2025 (+5% CAGR)
$ 0 billion
Clinical
end-points
LOAD / CPBI / VAS / NRS
150
Dogs patients with OA treated with VBX-2000 from now on
16
Sites involved in our clinical trials accross Europe

CLINICAL TRIALS

Osteoarthritis is a significant cause of pain, lameness and morbidity in dogs and many others species, including humans. It is a multi-factorial, progressive, degenerative disease of synovial joints, affecting not only the articular cartilage but also other structures within the specific synovial joint. Degradation of articular cartilage, subchondral bone sclerosis, osteophytosis, varying degrees of synovitis, meniscal and ligament degeneration are all characteristics of the disease process. Existing therapeutic arsenal available for canine and feline OA are exclusively pain/symptomatic treatments : there is a crucial need for new treatment targeting joint/cartilage degradation.

VBX-2000 is currently assessed in a regulatory, multricentric (Europe), randomized, double-blind, placebo-control, dose-ranging Pilot Clinical Study.

10 to 20%
Potential market share of VBX-2000 on the OA veterinary market
1st
First-in-class drug candidates
2029
Potential market approval in EU-US

VBX-2000 in Nutshell

VBX-1000

No treatment available for veterinary periodontitis
0
Dogs & Cats over 3 years old suffer from PD
0 %
annual forecast global pet dental therapeutic market targeted by VBX-1000 by 2035
$ 0 billion

VBX-1000 is a patented, first-in-class, oral small molecule, Cathepsin-K inhibitor for Periodontitis treatment. VBX-1000 is currently in development by Vetbiolix to obtain regulatory approval as the first veterinary treatment of Periodontitis (PD) in companion animals.

Periodontal disease (PD) is the most widespread oral disease in dogs, with studies showing that 60–97% of dogs have some degree of PD (1–4). PD is defined as plaque-induced immune-mediated damage to the periodontium, which anchors the tooth in the maxillary and mandibular bones. If left untreated, PD becomes a slowly evolving chronic inflammatory disease that first affects the gingiva (gingivitis) and then propagates to deeper structures of the periodontium, leading to progressive tooth attachment loss due to damage to the periodontal ligaments and loss of alveolar bone (periodontitis).

CLINICAL TRIALS

Vetbiolix launched in 2024 a proof-of-concept (PoC) clinical study assessing the efficacy and safety of VBX-1000 in client-owned dogs with spontaneously developed mild to moderate PD. The results provide initial evidence of the efficacy of once-a-day oral administration of VBX1000 for 90 days against major clinical manifestations of PD, supporting the regenerative action of VBX-1000 against alveolar bone loss. With the safety profile observed throughout the treatment period, these results support further development of VBX-1000 in this indication.

VBX-1000 is currently assessed in a regulatory, multricentric (Europe), randomized, double-blind, placebo-control, dose-ranging Pilot Clinical Study.

Clinical
end-points
CAL / PPD / Imaging
100
Dogs patients treated with VBX-1000 by end-2026
10
Sites involved in our clinical trials accross Europe
1st
Potential 1st therapeutic treatment of PD on the vet market
40 to 60%
Potential market share of VBX-1000 on the PD vet market
2030
Potential market approval in EU-US

VBX-1000 in Nutshell