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10/8 16:45 af Helge Larsen/PI-redaktør |
This session is over.
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10/8 16:45 af Jan Van de Winkel |
We look forward to 'speaking' with you again, thank you for the very interesting questions..
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10/8 16:45 af Helge Larsen/PI-redaktør |
Jan and David. Thank You for joining us and thank you for the many fullfilling answers to our questions. We look forward to to seeing you back here on ProInvestor.com after Q3.
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10/8 16:44 af Jan Van de Winkel |
This collaboration is progressing well and further updates should come from Novo Nordisk..
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10/8 16:44 af Jedi |
Could you please provide an update of the collaboration with Novo?
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10/8 16:43 af Jan Van de Winkel |
We expect to treat the first patients in the second half of the year and possibly see early data in 2017..
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10/8 16:42 af investor1989 |
What is the timeframe for the first AXL-ADC data after the IND ? Will it take long time because of toxicity (like TF-ADC) or have you some abbilities to move a little quicker forward with AXL
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10/8 16:42 af Jan Van de Winkel |
Great, fire away!
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10/8 16:42 af Helge Larsen/PI-redaktør |
Great. We have 2 questions more left for you.
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10/8 16:42 af Jan Van de Winkel |
This is currently not in the planning we believe revlimid to be an excellent combi partner with daratumumab as already shown in the POLLUX study..
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10/8 16:41 af biowolf |
will you be doing a head to head trial against revlimid?
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10/8 16:41 af Jan Van de Winkel |
We believe that daratumumab activates the immune system, in a different way than any of the traditional checkpoint blockers, and as such would be an ideal combo partner for potentially all other checkpoint blockers..
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10/8 16:40 af Jedi |
Has the recent failure of Opdivo changed your view on which checkpoint inhibitor would be a favorable combination with Darzalex?
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10/8 16:39 af Jan Van de Winkel |
Novartis is an active user of the DuoBody technology, we have been particularly impressed by the speed of Janssen in their DuoBody programs..
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10/8 16:38 af investor1989 |
The Novartis Duobody agreement started 2 months before the Jannsen agreement, but Jannsen has already 3 drugs in the clinic. What is status on the Novartis agreement ?
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10/8 16:38 af Jan Van de Winkel |
The data with Opdivo in frontline NSCLC were surprising and we await to see the further analysis by BMS. We are a strong believer in the potential of immuno oncology..
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10/8 16:37 af Jedi |
What are the key learnings from the somewhat surprising failure of Opdivo as frontline therapy in lung cancer?
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10/8 16:37 af Jan Van de Winkel |
Gilead is a very active user of the DuoBody platform..
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10/8 16:36 af Helge Larsen/PI-redaktør |
Question on behalf of pcf: "What I would like to know is what is the status with Gilead? They apearred omn a slide in January but I haven't heard anything important after that. I believe they have been snooping around for at least a year and a half right now” .
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10/8 16:36 af Jan Van de Winkel |
This would be broadly positive but we believe the real value for ofatumumab in the future to lie within the autoimmune disease area, where the value can be very significant..
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10/8 16:35 af Sukkeralf |
Could approval of Arzerra in combination with FC in relapsed CLL lift the sale significant?
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10/8 16:35 af Jan Van de Winkel |
We have accelerated the DuoBody CD3xCD20 program by several months and expect the first patients to be treated during 2017..
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10/8 16:34 af Sukkeralf |
Novartis just partnered up with Xencor on bispecific antibodies - and is moving their CD20/CD3 in the clinic this year. Is that why we see the acceleration of Humax-CD20/CD3 and when do you anticipate it to enter the clinic if everything goes according to plan H1 2017 or H2 2017 ?
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10/8 16:34 af Jan Van de Winkel |
We anticipate more DuoBody milestones in Q3, and up to now we have received around 67 M USD from DuoBody agreements and expect more to come..
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10/8 16:33 af Helge Larsen/PI-redaktør |
Sorry for the delay.
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10/8 16:32 af Sukkeralf |
Genmab recieved a milestone when the first participants were dosed with JNJ-61178104. For JNJ-61186372 and JNJ-63709178 the first patient has been dosed so could we expect 2 milestones here pretty soon (maybe after 3 or 5 patients are dosed) ?
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10/8 16:31 af Jan Van de Winkel |
Are there any more questions coming?
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10/8 16:26 af Jan Van de Winkel |
The partnerships with blue chip companies simply take time to negotiate and execute, we are confident to enter into new agreements in the coming time..
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10/8 16:25 af dingleberry |
Dear Jan, thx for taking my question. For some time we have waited for new duo- and hexa deals. Are potential partners not willing to accept the new strategy for increased GEN owership in the programs?
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10/8 16:25 af Jan Van de Winkel |
We currently think that tumors with high levels of expression of tissue factor (the target of tisotumumab vedotin) are likely to be optimal for this therapy..
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10/8 16:24 af Stroka |
How many kinds of tumors do you think Tisotumab effectively can crack down. Is there any common features of these tumors?
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10/8 16:23 af Jan Van de Winkel |
We believe BMS is focusing on HuMax-IL8 in clinical studies in combination with key checkpoint blocking antibodies..
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10/8 16:22 af Sukkeralf |
What kind of milestone package and royalty can we expect from Humax-IL8 program. Cormorant also looked at Humax-IL8 as one part of a bispecific antibody (DuoBody) - could it be something BMS would look at again ?
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10/8 16:22 af Jan Van de Winkel |
We still anticipate sharing some data this year and a more full data set in 2017..
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10/8 16:22 af investor1989 |
When are we seeing data for TF-ADC ? You said H2 2016. Will it bee preliminary data at ASH 2016 and then full data at ASCO 2017 ?
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10/8 16:21 af Jan Van de Winkel |
There are a number of potential solid tumor indications..
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10/8 16:20 af Jedi |
Which indication(s) is/are the object(s) of the first AXL-ADC study?
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10/8 16:19 af Jan Van de Winkel |
We have continuous interactions with all key pharma and biotech companies on several of our preclinical programs. For example the HexaBody DR5/DR5 program receives a lot of interest from key players based on solid preclinical data. At this stage we intend to hold on to 100% of the product rights.
.
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10/8 16:17 af dingleberry |
In the fall of 2014, you mentioned that big pharma wanted to partner up on the humax-axl-adc program based on pre-clinical data. What are the programs that attract the most interest from big pharma currently?
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10/8 16:17 af Jan Van de Winkel |
We have collected a very strong package of preclincal data that shows potent cancer cell killing ability..
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10/8 16:16 af Stroka |
You often describe Humax-Axl-Adc as very "potent". In what ways is the drug "potent" here in the very early stage?
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10/8 16:15 af Jan Van de Winkel |
We are very excited about the potential stimulating effect by daratumumab on T-Cells in cancer patients and thrilled to see new studies by Janssen, Genentech and Celgene combining checkpoint blockers with daratumumab in various cancers, including a solid tumor..
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10/8 16:14 af Budweis |
In the July edition of Blood Magazine a research team posted a very interesting article focusing on a previously unknown, multidimensional, immunomodulatory role of daratumumab. It sounds amazing! How do you see the possibilities and what are your next steps?
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10/8 16:13 af Jan Van de Winkel |
We would very much hope to see an update on the sc development at the next ASH..
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10/8 16:13 af Bulder |
Can we expect results from the sc dara trial at the next ASH?
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10/8 16:12 af Jan Van de Winkel |
Based on strong preclinical data set we are optimistic about the potential of dara outside of MM, there are also currently a couple of ISS studies ongoing, in amyloidosis and we do expect updates on the activation of the immune system in patients treated with daratumumab in the coming months..
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10/8 16:10 af Bulder |
What are your thoughts about the possibilities for dara in other indications than MM?
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10/8 16:10 af Jan Van de Winkel |
We do expect the data from the POLLUX study to be published in a top medical journal shortly, and to see updates at ASH in December..
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10/8 16:09 af Helge Larsen/PI-redaktør |
Questions on behalf of "Bikube". In connection with the publication of Pollux trial we saw a graph that is wildly impressive. Pfs showed no progression in 6 months. Is that still the case, or do you know what the current pfs% is.
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10/8 16:08 af Jan Van de Winkel |
We do expect updates on the NHL studies this year..
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