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.€176.3m
Last close€0.71
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
Actual1.3(3.3)(28.9)
Relative *(2.9)(7.5)(35.2)

* % 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 13:16:08 GMT

Form 6-K TiGenix NV For: Mar 31

Thu, 09 Mar 2017 06:11:15 GMT

TiGenix NV (Nasdaq: TIG) to Ring The Nasdaq Stock Market Closing Bell in ...

Thu, 15 Dec 2016 11:02:07 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. This will trigger a €15m milestone from Takeda, the European partner; Takeda views Cx601 as a breakthrough therapy. A Phase I/II trial using stem cells to control severe sepsis, a major unmet need, has just started. An interesting project is an acute cardiac stem cell therapy; full Phase I/II data is expected in H117. The 2016 US IPO raised €31m net.

Last updated on 02/03/2017

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 14/02/2017

Latest video

Executive interview - TiGenix

Industry outlook

The 180-patient Phase I/II study, SEPCELL with placebo and active arms is underway. This will be in intensive-care patients with severe community-acquired bacterial pneumonia or other pneumonia. The dose will be 160m eASC given on the first and third days of treatment in addition to standard of care. In the ongoing cardiac stem cell trial after acute AMI, six-month initial data showed no mortality from any cause or major adverse cardiac events after 30 days.

Last updated on 02/03/2017

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