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RENE Reneuron Group Plc

3.05
0.00 (0.00%)
Last Updated: 01:00:00
Delayed by 15 minutes
Share Name Share Symbol Market Type Share ISIN Share Description
Reneuron Group Plc LSE:RENE London Ordinary Share GB00BF5G6K95 ORD 1P
  Price Change % Change Share Price Bid Price Offer Price High Price Low Price Open Price Shares Traded Last Trade
  0.00 0.00% 3.05 - 0.00 01:00:00
Industry Sector Turnover Profit EPS - Basic PE Ratio Market Cap
Pharmaceutical Preparations 530k -5.41M -0.0946 -0.32 1.74M
Reneuron Group Plc is listed in the Pharmaceutical Preparations sector of the London Stock Exchange with ticker RENE. The last closing price for Reneuron was 3.05p. Over the last year, Reneuron shares have traded in a share price range of 2.95p to 10.25p.

Reneuron currently has 57,173,760 shares in issue. The market capitalisation of Reneuron is £1.74 million. Reneuron has a price to earnings ratio (PE ratio) of -0.32.

Reneuron Share Discussion Threads

Showing 5351 to 5370 of 8900 messages
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DateSubjectAuthorDiscuss
23/12/2016
10:49
Merry Christmas all and a happy, healthy and prosperous new year.
Whilst healthy is the most important, it would be nice to get an injection of proaperity.
Guess time will tell.
Good luck all.
Freddie

fredd1eboy
23/12/2016
09:56
as over 50% of the stop is owned by 3 fund managers legally committed to ensuring this doesn't happen unless friendly and fair

Exactly; Its easily a done deal, perhaps with a small premium

norbus
22/12/2016
07:36
Its a bit like doubting Thomas. Looks like market needs to be 100% certain, as currently no appetite for risk.Hopefully Renes 2017 results will calm fears. Time will tell
fredd1eboy
22/12/2016
07:33
Rene cannot be taken out on the cheap, as over 50% of the stop is owned by 3 fund managers legally committed to ensuring this doesn't happen unless friendly and fair!
fredd1eboy
22/12/2016
07:01
The share price is worrying for 2 reasons

1. Could it be that Rene is being prepared for a cheap takeout?
2. Could it be that progress is not rated by those in the know?

norbus
21/12/2016
07:47
Cheers. The more patient stories the better.
waterloo01
20/12/2016
21:20
Excellent patient driven article. Very positive and c/o flier lse site




Best wishes.
Freddie

fredd1eboy
06/12/2016
10:56
Waterloo01

I suspect the placebo will be done in the way it has for the trial of another neuro surgical procedure i.e. the placebo patients will be prepared for the surgical procedure and then have a small incision so that they are unaware that they haven't had the full procedure.

It is amazing how often there is a real placebo affect.

Having said that I have first hand experience of a close relative who has suffered a major stroke six months ago and would say that a 75% chance of some clinical improvement seems to be well worth trying given the only treatment option is physiotherapy with diminishing returns as time goes on.

pj84
06/12/2016
10:19
Having this kind of brain op is really no big deal these days. It's not as if they, as in some procedures, saw the top of your skull off and expose the entire cerebral hemispheres, lift them up and play with the bits underneath. No, a small hole is drilled through the skull and a very fine needle delivers the stem cells. If you have lost the use of your hands and arms, I suspect that taking part in a randomised trial where you have a 50% chance of receiving the treatment (which so far has seen excellent results, so you have 50% x 75% = 37.5% overall chance of seeing significant benefits after 12 months) is the least of your worries. And it's actually better than this because, if the trial goes well, it is possible that it could be stopped early and, if you were one of the placebo groups, you would probably be transferred immediately over to the therapeutic. And, remember, just taking a pill in a trial can be very dangerous:
small crow
06/12/2016
09:43
Norbus, true. it's not like taking a pill, however there is also very little alternative for stroke patients. On placebo, I've no idea how this might be done in this treatment and one wonders if they can't use either a control group of similar size or natural history?

However they will need some sort of placebo as they will need to prove that the improvements seen are above the normal recovery curve.

I guess I'm starting to understand the market reaction as I also hoped to see clearer transformative progression, although the 75% seeing clinical benefit is - on the surface - rather good.

waterloo01
06/12/2016
09:02
Waterloo01

Messing inside brains is dangerous and expensive; The pull to go for treatment needs to be really convincing for there to be a serious market against alternate choice

norbus
05/12/2016
19:12
Some interviews with one of the 4 might also help bring it into focus.
waterloo01
05/12/2016
19:04
Waterloo01 - good points I agree. You've literally laid out all the points I had in mind. I do find it strange when companies fail to promote their good news in the most effective positive fashion. What do they employ brokers and PR companies for for heavens sake!! What a waste of money PR is in my investing experience. Clueless.

And yes there is a seller out there and they have largely caused the brakes to be slammed on the share price IMO. The great unknown is how much more stock they want to shift. If it's not too big then we might find the share price starting to elevate in the next few days or weeks. Perfectly possible as the news IS positive and the company has stacks of cash. A new II coming on board would help of course.

dibs61
05/12/2016
18:01
I guess it's the missed endpoint (because endpoint was after 3 months and they met it after the deadline) that has caused the initial reaction, but 4 of 21 patients (20%) made significant improvement in the main score.

If the end point had been longer, the headline would have been different, in patients who normally don't show much recovery.

I'd definitely have led with ...."In all, 15 out of 21 patients had a clinically significant response on at least one efficacy measure, with these improvements kept up throughout the follow-up period".

That's 75% did show a 'clinically significant response" and that's impressive.

waterloo01
05/12/2016
17:41
Thank you for your post, waterloo01, & I think you summarise the situation as well as can be. There's quite a limit to how insightful we can hope to get !
dogwalker
05/12/2016
17:23
Odd reaction to today's news. What would have happened if the trial had been negative!

My reading of the trial results was essentially very positive (especially for the 3/4 patients who had the best response), although I would have put the headline in the RNS that 15 of 21 had a meaningful clinical response. I guess some were expecting an instant fuller recovery from more patients? The company have always slated the need to do a placebo phase 3, so don't think that's it?

We do however seem to have a seller, which is odd as you would have thought they might have allowed a rise before cashing in.

Having said all that, I've known stocks to react days later to news, especially if a seller clears.

Any other insight from anyone?

waterloo01
05/12/2016
16:48
IP would be worth a huge amount if it was effective; You need to know what is out there against Rene. These companies are not asset strip jobs, they burn cash. and no company takes into account a shut down w/down Going Concern , if heavens forbid, nothing material is delivered
norbus
05/12/2016
15:50
Norbus - transparently uninformed and casual comment. Cash on the BS alone is worth at least 2p on the share price

So you are effectively valuing IP at ZERO or less. Not that you knew it clearly ...

dibs61
05/12/2016
15:06
More likely to drift to nearer 2 with not a great deal on the immediate horizon. They might do well to buy into another string to their bow whist they have cash
norbus
05/12/2016
13:01
British biotech ReNeuron has posted generally encouraging midstage data which showed their stem cell therapy could help certain stroke patients move their arms better, after being left disable by their condition. Despite not hitting its primary endpoint, it is still plotting a pivotal test starting next year.

Its CTX cell therapy candidate was being tested in a small, phase 2 trial, known as Pisces II, that worked as a single arm, open-label study in patients living with disability resulting from ischaemic stroke.

The study’s primary endpoint was relatively modest: It needed two patients, out of 21, to reach a minimum two-point improvement in what is known as the grasping and lifting test, a part of the Action Research Arm Test (ARAT), at three months after treatments.

In the end, three of the 21 patients achieved this at three, six or 12 months respectively after treatment, and were within a group of four responders who also showed “clinically relevant improvements” on the total ARAT score of arm motor performance.

But it missed its target as some responses came later than the three-month target. The biotech however still said that the result was “nonetheless highly encouraging,” and the market tended to agree, with its shares jumping over 22% on the news today.

This was also because “strongly positive results” were also reported in the other endpoints of the study, with seven patients (33%) showing a “clinically relevant improvement” on the Modified Rankin Scale (a measure of disability and dependence) and eight patients (38%) showing a clinically relevant improvement on the Barthel Index (a measure of performance in activities of daily living).

In all, 15 out of 21 patients had a clinically significant response on at least one efficacy measure, with these improvements kept up throughout the follow up period.

The company says that it will now seek a chat with the FDA and EMA about starting a randomised, placebo-controlled, pivotal trial in patients who are living with disability post-stroke.

Olav Hellebø, CEO of ReNeuron, said: “We are delighted that the Pisces II clinical trial has shown our CTX cell therapy candidate has the potential to become a treatment option for patients living with chronic consequences following stroke. We are particularly excited by the response rate seen on the measures relating to disability and activities of daily living, given that these are the most important for patients and their carers.”

Hellebø noted that these measures are also the ones viewed by regulatory authorities as most relevant for late-stage clinical development.

He added that the co has a “strong balance sheet” to fund its planned pivotal study.

Stem cell therapies, once seen as a great hope in the research filed for a variety of diseases, has in recent years been beset with testing setbacks, with progress in getting new therapies to market much slower than originally hoped for.

Back in the summer, Teva returned the full rights of a phase 3 experimental heart drug that back to Mesoblast as it walked away from development. And in the spring, CA-based BioCardia delayed its plans to raise $50 million for its stem cell research.

bigspuds
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