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101-120 of 5056
Drop to 350 ?
loss making
loss making
https://links.sgx.com/1.0.0/corporate-announcements/FMCPS3EGS4EDYWS4/37ad4b9f47c923f5130b771e450b9b7a9149abd3a919a8d1aee7f263062032f7
Good that you bring up about success rates. Traditionally big pharmas had been relying on these 40-60% success rates to grow their businesses! Pharmas know the % and had been investing in R& D as they know the returns are high.
if you had bother to research more, wafermine is based on ketamine and utilizing a new mode of administration. Ketamine is an existing medicine which is well proven to be safe.
phase II study does not require large patients. 100-200 are considered a lot. This is the norm.
in wafermine, it' s phase IIb study is well proven in efficacy and safety and that' s why US is investing in its further development, sparing Ixbiopharma the investment..
if you had bother to research more, wafermine is based on ketamine and utilizing a new mode of administration. Ketamine is an existing medicine which is well proven to be safe.
phase II study does not require large patients. 100-200 are considered a lot. This is the norm.
in wafermine, it' s phase IIb study is well proven in efficacy and safety and that' s why US is investing in its further development, sparing Ixbiopharma the investment..
kye_lin ( Date: 10-May-2026 12:28) Posted:
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If you believe in the stock and the narrative, go for it. The market will decide. To each his own.
By your theory beng Kuang loss result, Beng Kuang now should be 3 series too.
It?s a Pharma company without real sales since it?s not passed.
How to make profit from something that hasn?t been approved for usage?!
It?s a Pharma company without real sales since it?s not passed.
How to make profit from something that hasn?t been approved for usage?!
kye_lin ( Date: 09-May-2026 09:31) Posted:
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Beside full FDA approval, iX Biopharma is leveraging a JV with [Orion Specialty Labs] to introduce the drug via US compounding pharmacies, bypassing some traditional approval timelines.
There's much info on Wafermine...go check out ChatGPT or Copilot.
Then you will know why I am so confident.
Holding out for $1...haha
There's much info on Wafermine...go check out ChatGPT or Copilot.
Then you will know why I am so confident.
Holding out for $1...haha
Phase 3 trials failure rate is 40 to 50%. Large scale trials on actual patients. A lot failed due to unexpected side effects and poor real world efficacy of drug. Phase 2 trials is just proof of concept on a few hundred patients. Just saying.
Passing phase 2 does not mean automatic pass phase 3.
If so, no need to test anymore.
My last wword, no need to discourse anymore, wasteb of time, just wait for result.
If so, no need to test anymore.
My last wword, no need to discourse anymore, wasteb of time, just wait for result.
Why will confidence be misplaced? As long as wafermine is concerned, it has passed Phase II studies with good efficacy data as well as safety data. That' s why it is now moving to phase III study. This is typical route for any pharmaceuticals products.
Good thing this counter is generating more interest now. and hopefully people will read more into it rather than simply investing blindly.
Good thing this counter is generating more interest now. and hopefully people will read more into it rather than simply investing blindly.
ahberngh ( Date: 10-May-2026 11:26) Posted:
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I am saying that nothing is certain and we must not be overconfident.
But, yes, I have been following IX since I first bought into it
in Oct 2020 (and continuing to buy even now), and I am optimistic that it should pass the trial.
Let' s hope that our confidence is not misplaced.
But, yes, I have been following IX since I first bought into it
in Oct 2020 (and continuing to buy even now), and I am optimistic that it should pass the trial.
Let' s hope that our confidence is not misplaced.
stlimst ( Date: 10-May-2026 10:59) Posted:
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I am saying IX is almost certain to ace Phase 3 clinical trials.
Yes the trial is stringent and evidence based.
But UX is not new to this and have been priming for this one for quite some time.
The fact that they can convinced US DoD to fund this says alot.
No fear.
Yes the trial is stringent and evidence based.
But UX is not new to this and have been priming for this one for quite some time.
The fact that they can convinced US DoD to fund this says alot.
No fear.
ahberngh ( Date: 10-May-2026 09:52) Posted:
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There is no guarantee.
Yes, every chance will be given for it to pass since it has support of the Army,
but the phase 3 trial is based on scientific evidence and if the science fails, it won' t pass.
I will hope that the science won' t fail because I am vested.
Yes, every chance will be given for it to pass since it has support of the Army,
but the phase 3 trial is based on scientific evidence and if the science fails, it won' t pass.
I will hope that the science won' t fail because I am vested.
stlimst ( Date: 10-May-2026 08:41) Posted:
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One of the key milestone is the JV with Orion. Possibly to support the phase III study and subsequently to commercialize.
stlimst ( Date: 10-May-2026 08:41) Posted:
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Bro, with the funding and support from US government, phase 3 trial will pass, not 'if'.
There's already agreement for emergency use of the drug in US, while waiting for FDA.
Yes, this is game changing.
There's already agreement for emergency use of the drug in US, while waiting for FDA.
Yes, this is game changing.
ahberngh ( Date: 10-May-2026 07:48) Posted:
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Thanks for the correction.
Yes each country has their own approving authority.
But US FDA is like the standard bearer. Once you have US FDA approval, normally other approving authority will accept.
That's what I meant.
Yes each country has their own approving authority.
But US FDA is like the standard bearer. Once you have US FDA approval, normally other approving authority will accept.
That's what I meant.
Winall88 ( Date: 10-May-2026 00:08) Posted:
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The phase 3 trial if passed and FDA approval is granted
will be a game changer for IX.
A lot depends on this.
will be a game changer for IX.
A lot depends on this.
Overprice or not, 1 year later you will know hee hee hee....
makehay ( Date: 09-May-2026 22:00) Posted:
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Allow me to correct. Fast track FDA approval doesn' t mean can be sold worldwide. Other countries will need their local HSA approval before the drug can be sold in their countries. But US is the biggest market in the world, and having FDA approval means a lot. Other countries will use FDA' s label to apply their local licence.
stlimst ( Date: 09-May-2026 23:17) Posted:
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The game changer is Wafermine - the product that US DoD is funding the clinical trials. The critical FDA's approval is also being fast track.
Once you obtain FDA approval. The drug can be sold worldwide.
Once you obtain FDA approval. The drug can be sold worldwide.
Overpriced. Still loosing money. the Neutriceuticals NAD stuff, revenue is pathethic, considering the glowing write up. All the hype is on the US military contract for stage 3 development.
PQTPQK ( Date: 09-May-2026 18:31) Posted:
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