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Ablynx N.V.. (3/2/18). "Press Release: Ablynx Commences Dosing in Its Phase II Study of ALX-0171 in Hospitalised Japanese Infants with a RSV Infection". Ghent.

Region Region Japan
Organisations Organisation Ablynx N.V. (Euronext Brussels: ABLX, Nasdaq: ABLX)
  Group Sanofi (Group) [since May 2011]
  Organisation 2 Consilium Strategic Communications Ltd. (CSC)
Products Product ALX-0171 (anti-RSV Nanobody)
  Product 2 clinical research
Persons Person Zeldin, Robert K. (Ablynx 201608 CMO)
  Person 2 Gardner, Philippa (Consilium 201705– joins London CSC office before Lehman Brothers + Jefferies + Edison)

Ablynx [Euronext Brussels and Nasdaq: ABLX] today announced that the first patient has been dosed in the Japanese Phase II study of ALX-0171, the Company’s wholly-owned inhaled Nanobody® to treat respiratory syncytial virus (RSV) infections.

This Phase II study is a randomised, double-blind, placebo-controlled, multi-centre study of ALX-0171 in 60 Japanese infants (aged 1-24 months) diagnosed with RSV and hospitalised for a lower respiratory tract infection. The study will evaluate four different doses and a safety review by an independent Data Monitoring Committee will occur prior to proceeding to each higher dose. ALX-0171 will be administered via nebulisation once daily for three consecutive days and will be given along with standard-of-care treatment.

The primary objectives of this Phase II study are to evaluate the safety, tolerability and systemic pharmacokinetics (PK) of different doses of inhaled ALX-0171 in Japanese infants infected with RSV. Secondary objectives include the evaluation of the antiviral effect, clinical activity, immunogenicity and pharmacodynamics (PD) of different doses of inhaled ALX-0171. The study is expected to read out in the second half of 2019.

Dr Robert K. Zeldin, Chief Medical Officer at Ablynx, commented: “We are very pleased to start this Phase II study of ALX-0171 in RSV-infected Japanese infants and look forward to reporting the results in the second half of 2019. There remains an urgent need for effective therapies in RSV and this is an important step in making our inhaled anti-RSV Nanobody available to patients worldwide. This year, we also plan to report the topline results from our global Phase IIb RESPIRE study in 180 RSV-infected hospitalised infants.”

About RSV

Respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract infections and the leading viral cause of severe lower respiratory tract disease in infants and young children worldwide. It is the primary cause of infant hospitalisation and virus-associated deaths in infants, with estimated global annual infection of 33 million and hospitalisation rates of 3-4 million1. It is associated with an estimated 3,000-8,500 deaths in infants <2 years globally per year2, and it has been linked to an increased risk of asthma development later in life3.

Current treatment of RSV infections is primarily focused on symptomatic relief, hence the need for an effective and specific anti-RSV therapeutic.

About ALX-0171

ALX-0171 is a wholly-owned trivalent Nanobody that binds to the F-protein of RSV, thereby inhibiting viral replication and neutralising RSV activity by blocking virus uptake into cells. The physical robustness of the Nanobody allows administration via inhalation directly to the site of infection, i.e. the respiratory tract. ALX-0171 has shown a potent anti-viral effect against a broad range of RSV strains in vitro and it has demonstrated a marked therapeutic effect following administration via nebulisation in a neonatal animal model for infant RSV infection4.

Repeated daily inhalation of ALX-0171 was proven to be well-tolerated in multiple Phase I clinical studies in adults and a Phase I/IIa study in 53 hospitalised infants (aged 1-24 months) with a RSV infection. In addition, repeated daily inhalation of ALX-0171 had an immediate and significant impact on viral replication and an encouraging initial therapeutic effect in the Phase I/IIa study.

A randomised, double-blind, placebo-controlled, international, multi-centre dose-ranging Phase IIb study (RESPIRE) of three different doses of inhaled ALX-0171 in 180 hospitalised infants (aged 1-24 months) with a RSV infection is currently ongoing. The sequential dose escalation part, which enrolled 36 infants, has been completed in July 2017, after which the Data Monitoring Committee recommended to continue the study without changes to the protocol. The parallel dose part of the study in 144 infants was initiated in August 2017. The primary endpoint of the trial is to evaluate the anti-viral effect of treatment measured in samples taken by nasal swabs. Secondary endpoints include safety, pharmacokinetics and clinical activity determined by assessment of the composite Global Severity Score. Topline results from the RESPIRE trial are expected in H2 2018.

About Ablynx

Ablynx is a biopharmaceutical company engaged in the development of Nanobodies, proprietary therapeutic proteins based on single-domain antibody fragments, which combine the advantages of conventional antibody drugs with some of the features of small-molecule drugs. Ablynx is dedicated to creating new medicines which will make a real difference to society. Today, the Company has more than 45 proprietary and partnered programmes in development in various therapeutic areas including inflammation, haematology, immuno-oncology, oncology and respiratory disease. The Company has collaborations with multiple pharmaceutical companies including AbbVie; Boehringer Ingelheim; Eddingpharm; Merck & Co., Inc., Kenilworth, New Jersey, USA; Merck KGaA; Novo Nordisk; Sanofi and Taisho Pharmaceuticals. The Company is headquartered in Ghent, Belgium. More information can be found on

1 Shi et al, Lancet 2017
2 Byington et al, Pediatric 2014
3 Sigurs et al, Thorax 2010; Backman et al, Acta Pediatr 2014
4 Oral presentation at the 9th International RSV Symposium, November 2014

For more information, please contact:


Dr Edwin Moses CEO t: +32 (0)9 262 00 07 m: +32 (0)473 39 50 68 e:
Lies Vanneste Director IR t: +32 (0)9 262 0137 m: +32 (0)498 05 35 79 e:

Ablynx media relations:

Consilium Strategic Communications Mary-Jane Elliott, Philippa Gardner, Sukaina Virji t: +44 (0)20 3709 5700 e:

Joele Frank, Wilkinson Brimmer Katcher Dan Katcher or Joseph Sala t: +1 212-355-4449


Certain statements, beliefs and opinions in this press release are forward-looking, which reflect the Company or, as appropriate, the Company directors’ current expectations and projections about future events. By their nature, forward-looking statements involve a number of risks, uncertainties and assumptions that could cause actual results or events to differ materially from those expressed or implied by the forward-looking statements. These risks, uncertainties and assumptions could adversely affect the outcome and financial effects of the plans and events described herein. A multitude of factors including, but not limited to, changes in demand, competition and technology, can cause actual events, performance or results to differ significantly from any anticipated development. Forward looking statements contained in this press release regarding past trends or activities should not be taken as a representation that such trends or activities will continue in the future. As a result, the Company expressly disclaims any obligation or undertaking to release any update or revisions to any forward-looking statements in this press release as a result of any change in expectations or any change in events, conditions, assumptions or circumstances on which these forward-looking statements are based. Neither the Company nor its advisers or representatives nor any of its parent or subsidiary undertakings or any such person’s officers or employees guarantees that the assumptions underlying such forward-looking statements are free from errors nor does either accept any responsibility for the future accuracy of the forward-looking statements contained in this press release or the actual occurrence of the forecasted developments. You should not place undue reliance on forward-looking statements, which speak only as of the date of this press release.

Record changed: 2018-03-08


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