TiGenix (TIGB)

Business description

TiGenix is a Belgian-Spanish company using allogeneic adipose stem cells to aid healing of complex perianal fistulas in Crohn’s disease (EU approval ongoing with Takeda as the European partner. Sepsis and cardiac stem cell therapies are in development

Stock data

Market cap.€194.7m
Last close€0.75
High / Low (52 weeks)€1.1 / €0.6
Stock market listingEU
Forecast net debt (€m)14.5
Forecast gearing ratio (%)86
TeamHealthcare
SectorPharmaceutical & healthcare

Price performance

%1m3m12m
Actual3.26.8(18.8)
Relative *2.91.7(24.8)

* % Relative to local index

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Company news

TiGenix NV (TIG), Interview with Eduardo Bravo, CEO

Mon, 23 Jan 2017 20:03:45 GMT

BRIEF-Tigenix NV announces top-line one-year results from Caremi clinical trial

Mon, 13 Mar 2017 06:00:00 GMT

Canaccord Genuity Starts TiGenix NV (TIG) at Buy

Mon, 09 Jan 2017 13:07:30 GMT

Nasdaq Welcomes TiGenix NV (Nasdaq: TIG) to The Nasdaq Stock Market

Thu, 15 Dec 2016 22:18:45 GMT

TiGenix to participate in key investor conferences in April 2017

Wed, 05 Apr 2017 04:52:30 GMT

Investment summary

TiGenix is set for a decisive 2017 with possible EU approval in H2 of the allogeneic stem cell therapy Cx601 to treat complex perianal fistulas in Crohn’s disease. Day 180 questions have been received. An approval triggers a €15m milestone from Takeda, the European partner; Takeda views Cx601 as a breakthrough therapy. A Phase I/II trial in severe sepsis has started. Data from the acute cardiac stem cell therapy project have been reported. The 2016 US IPO raised €31m net.

Last updated on 04/04/2017

Y/E Dec Revenue (€m) EBITDA (€m) PBT (€m) EPS (c) P/E (x) P/CF (x)
2013A 0.9 (12.4) (14.8) (10.8) N/A N/A
2014A 0.8 (14.5) (15.9) (9.8) N/A N/A
2015E 1.8 (14.6) (17.3) (10.0) N/A N/A
2016E 2.1 (17.0) (20.5) (12.2) N/A N/A

Last updated on 21/03/2017

Latest video

Executive interview - TiGenix

Industry outlook

The 180-patient, placebo-controlled study Phase I/II study in severe sepsis, SEPCELL is underway in intensive-care patients with severe community-acquired bacterial pneumonia or other pneumonia. The total dose will be 160m eASC given in two doses in addition to standard of care. In the cardiac stem cell trial after acute AMI, final data showed no mortality from any cause or any major adverse cardiac events but gave a positive safety outcome with a possible signs of smaller infarct sizes in a subgroup.

Last updated on 04/04/2017

Key management

Willy Duron, Chairman
Eduardo Bravo, CEO
Claudia D’Augusta, CFO

Company address

Research Park Haasrode 1724
Romeinse straat 12 bus 2
B - 3001 L
Belgium
+32 16 39 60 60
View website