ReNeuron Group (RENE)

Business description

ReNeuron is a UK biotech company developing allogeneic cell therapies: CTX neural stem cell products for stroke disability (Phase IIa) and critical limb ischaemia (Phase I); and human retinal progenitor cells for retinitis pigmentosa (Phase I/II).

Stock data

Market cap.£74.4m
Last close2.35p
High / Low (52 weeks)3.7p / 2.3p
Stock market listingLN
Forecast net cash (£m)49.4
Forecast gearing ratio (%)N/A
TeamHealthcare
SectorPharmaceutical & healthcare

Price performance

%1m3m12m
Actual(9.6)(10.5)(30.4)
Relative *(10.6)(14.1)(40.7)

* % Relative to local index

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Company news

ReNeuron makes a guest appearance on BBC2

Wed, 15 Feb 2017 08:03:45 GMT

ReNeuron chief delighted with latest stroke data

Mon, 05 Dec 2016 08:25:11 GMT

ReNeuron Group will hit "milestone" with results next year, says CEO

Tue, 06 Sep 2016 08:50:34 GMT

ReNeuron makes strong start to key trial period

Wed, 07 Dec 2016 13:07:30 GMT

ReNeuron Group PLC treats first patient in retinitis pigmentosa trial

Tue, 15 Mar 2016 09:49:08 GMT

Investment summary

ReNeuron reported in December 2016 positive Phase II trial data for its CTX cells in chronic stroke patients, despite not meeting the three-month time frame of a two-point improvement in its primary outcome measure, the Action Research Arm Test (ARAT). As a result, the company has confirmed that it will progress to a pivotal controlled clinical study in 2017. Beyond CTX, we expect safety and efficacy data from its retinitis pigmentosa (RP) trial in 2017 and Phase I data from its critical limb ischaemia (CLI) trial. Our rNPV has increased to £291m.

Last updated on 23/03/2017

Y/E Mar Revenue (£m) EBITDA (£m) PBT (£m) EPS (p) P/E (x) P/CF (x)
2015A 0.0 (10.3) (10.3) (0.50) N/A N/A
2016A 0.0 (13.6) (12.8) (0.44) N/A N/A
2017E 0.0 (19.9) (19.5) (0.58) N/A N/A
2018E 0.0 (31.5) (31.3) (0.93) N/A N/A

Last updated on 23/03/2017

Latest video

Executive Interview - ReNeuron

Industry outlook

Stroke is a high-risk indication, but ReNeuron is attempting to demonstrate a meaningful reduction in disability that would offer a compelling case for further development and/or partnering. Initial three month follow-up data from its Phase IIa stroke study was presented at H117 results, which were sufficiently strong for the Company to plan to progress to a pivotal controlled clinical study in 2017. The hRPC programme has Orphan (EU/US) and Fast Track (US) designation with a potentially pivotal Phase II/III study planned for 2018.

Last updated on 02/03/2017

Key management

John Berriman, Chairman
Olav Hellebø , CEO
Michael Hunt, CFO
John Sinden, Chief Scientific Officer

Company address

Pencoed Business Park
Pencoed
Bridgend
CF35 5HY
United Kingdom
+44 (0)1483 302560
View website