Oryzon Genomics — A year of data readouts

Oryzon Genomics (BME: ORY)

Last close As at 20/12/2024

EUR1.55

−0.05 (−2.89%)

Market capitalisation

EUR102m

More on this equity

Research: Healthcare

Oryzon Genomics — A year of data readouts

Oryzon has a total of five Phase II studies ongoing with its two lead assets iadademstat (formerly ORY-1001) and vafidemstat (formerly ORY-2001), which are all expected to have preliminary data readouts in 2019. In November 2018, the company announced the first patients had been recruited in to the iadademstat Phase IIa small cell lung cancer (CLEPSIDRA) and acute myeloid leukaemia (ALICE) studies. A scientific paper was recently published by a third party in Science Signalling, which has revealed a potential mechanism of action of iadademstat (ORY-1001) in pre-clinical SCLC models; this is supportive to Oryzon’s ongoing Phase II study in SCLC. Our valuation is slightly higher at €364m or €9.3/share.

Analyst avatar placeholder

Written by

Healthcare

Oryzon Genomics

A year of data readouts

Q418 update

Pharma & biotech

27 February 2019

Price

€3.71

Market cap

€145m

US$1.14/€

Net cash (€m) at end Q418

16.2

Shares in issue

39.1m

Free float

71%

Code

ORY

Primary exchange

Madrid Stock Exchange

Secondary exchange

N/A

Share price performance

%

1m

3m

12m

Abs

30.9

29.3

43.1

Rel (local)

30.3

27.4

53.5

52-week high/low

€5.0

€2.1

Business description

Oryzon Genomics is a Spanish biotech focused on epigenetics. Iadademstat (Phase IIa) is being explored for acute leukaemias and SCLC; vafidemstat, its CNS product, is in Phase IIa trials in MS, AD and aggression. Newer asset ORY-3001 is being developed for certain orphan indications.

Next events

First readouts from Phase IIa study with vafidemstat in aggression

Q219

First readouts from Phase IIa studies with iadademstat in AML, SCLC

Q219

Preliminary readouts from Phase IIa studies with vafidemstat in AD and MS

H219

Analysts

Jonas Peciulis

+44 (0)20 3077 5728

Alice Nettleton

+44 (0)20 3077 5700

Oryzon Genomics is a research client of Edison Investment Research Limited

Oryzon has a total of five Phase II studies ongoing with its two lead assets iadademstat (formerly ORY-1001) and vafidemstat (formerly ORY-2001), which are all expected to have preliminary data readouts in 2019. In November 2018, the company announced the first patients had been recruited in to the iadademstat Phase IIa small cell lung cancer (CLEPSIDRA) and acute myeloid leukaemia (ALICE) studies. A scientific paper was recently published by a third party in Science Signalling, which has revealed a potential mechanism of action of iadademstat (ORY-1001) in pre-clinical SCLC models; this is supportive to Oryzon’s ongoing Phase II study in SCLC. Our valuation is slightly higher at €364m or €9.3/share.

Year end

Revenue (€m)

PBT*
(€m)

EPS*
(€)

DPS
(€)

P/E
(x)

Yield
(%)

12/17

4.3

(4.6)

(0.14)

0.0

N/A

N/A

12/18

6.8

(3.7)

(0.03)

0.0

N/A

N/A

12/19e

6.1

(6.8)

(0.17)

0.0

N/A

N/A

12/20e

6.1

(6.8)

(0.17)

0.0

N/A

N/A

Note: *PBT and EPS are normalised, excluding amortisation of acquired intangibles, exceptional items and share-based payments.

All Phase II studies now ongoing, waiting for data

With the first patients now recruited into the new iadademstat Phase IIa SCLC (CLEPSIDRA) and AML (ALICE) studies, all Phase II studies have now commenced and recruitment is progressing. The first preliminary readouts will come in Q219 from the ongoing vafidemstat REIMAGINE study (likely at the European Congress of Psychiatry in early April 2019), iadademstat CLEPSIDRA study (likely at ASCO in June 2019) and iadademstat ALICE study (likely at EHA in June 2019). This will be followed by further multiple readouts from the vafidemstat SATEEN and ETHERAL studies in H219.

Financials: Cash reach to late 2020

Oryzon reported an operating loss of €2.9m in 2018, compared to €4.3m in 2017, which was better than our expected €5.6m. This was mainly due to a combination of slightly lower capitalisation of R&D spend and lower R&D expenses of €7.4m in 2018 vs our expected €8.5m (Oryzon reports using local GAAP and capitalised R&D costs are included as income in EBIT, which was €6.8m in 2018). Oryzon had cash and cash equivalents of €34.5m at the end of Q418 and our fine-tuned total operating loss estimates for 2019 and 2020 are €6.2m and €6.3m, respectively. The y-o-y increase from FY18 is mainly due to more intensive R&D activities expected as the pipeline matures. According to our model, cash reaches in well into H220, in line with management’s guideline (Q420).

Valuation: €364m or €9.3/share

Our valuation is up slightly at €364m or €9.3/share from €342m or €8.7/share due to rolling our model forward. The reported year-end cash position was €34.5m (cash and short-term investments; net cash €16.2m). Because Oryzon’s clinical trials are progressing as planned across all indications, we leave our assumptions unchanged. Data readouts from the ongoing five clinical trials will provide multiple catalysts for the share price this year (detailed below).

Maturing R&D pipeline

Exhibit 1: Oryzon’s R&D pipeline

Product

Indication and stage

Mechanism of action

Notes

Iadademstat (ORY-1001)

AML, Phase IIa ALICE trial in combination with azacitidine

SCLC, Phase IIa CLEPSIDRA trial in combination with platinum-etoposide

Small molecule LSD1 inhibitor - LSD1 is a histone eraser enzyme that removes methyl groups

Oryzon reported supportive Phase I/IIa data in acute leukaemia at the ASH conference in December 2016.

Two new Phase IIa trials have been initiated in AML (ALICE) and SCLC (CLEPSIDRA). First readouts from both trials expected in late Q219.

Vafidemstat (ORY-2001)

AD, Phase IIa ETHERAL trial, monotherapy

MS, Phase II SATEEN trial, monotherapy

Aggression, Phase IIa REIMAGINE trial, monotherapy

Small molecule LSD1 and MAOB inhibitor

Reported Phase I safety and PK/PD data from healthy volunteers on 31 March 2017 at the ADPD conference.

Oryzon initiated clinical trials in MS (SATEEN) and AD (ETHERAL). Preliminary readouts expected in H219.

Basket trial REIMAGINE in aggression in several neuropsychiatric disorders initiated. Preliminary readout expected Q219, followed by more readouts throughout 2019.

ORY-3001

Undisclosed non-oncological diseases

Small molecule LSD1 inhibitor

Initial positive preclinical data published in sickle cell disease, but further development not disclosed yet. Successfully completed regulatory toxicology.

Source: Edison Investment Research, Oryzon Genomics;

Vafidemstat: Preliminary readouts from aggression basket trial start in Q219

The first preliminary data readouts in 2019 will be from the REIMAGINE basket aggression trial with vafidemstat (ORY-2001), the lead CNS asset a dual LSD1/MAOB inhibitor. According to Oryzon’s updated R&D newsflow (Exhibit 2), there will be several sequential preliminary readouts from the trial starting in Q219 (potentially at the European Congress of Psychiatry in Warsaw on 6–9 April 2019) and throughout the year. The single-arm, open-label study is being carried out at the Hospital Vall d’Hebrón in Barcelona and is enrolling at least six patients per indication: Alzheimer’s disease, dementia with Lewy bodies, attention deficit hyperactivity disorder, autism spectrum disorder and borderline personality disorder. The open-label treatment with ORY-2001 will last for eight weeks with the last patient out expected in Q119. The main goal is the assessment of reduction in aggression.

Exhibit 2: Vafidemstat near-term catalysts

Source: Oryzon

The REIMAGINE trial with vafidemstat is a so-called basket trial (Exhibit 3 details the study design), which employs an innovative design borrowed from drug development in oncology. Aggression is often seen in a variety of neurodegenerative and neuropsychiatric conditions and vafidemstat has demonstrated holistic effects in this regard in preclinical models (for a more detailed overview see our outlook report).

For now precise details about what kind of data will be released have not been disclosed, but the rationale of the trial is to look for signals of efficacy in one or more indication, then decide which setting in psychiatry is best suitable for more advanced trials. Once the data are released and further development is clarified, we will revisit our ORY-2001 valuation model, potentially adding indications beyond current ones Alzheimer’s disease and multiple sclerosis.

Exhibit 3: Oryzon’s vafidemstat (ORY-2001) REIMAGINE study (Eudra CT number: 2018-002140-88)

Summary design

A single centre, open-label, one-arm, eight-week study to evaluate the efficacy, safety and tolerability of ORY-2001 in aggression in adult population with Alzheimer’s disease (AD), Lewy Body Dementia (LBD), Adult attention Deficit Hyperactivity Disorder (ADHD) Borderline Personality Disorder (BPD), Autism Spectrum Disorder (ASD)

Treatment groups

Treatment arm: vafidemstat 1.2mg

(Single arm, no placebo control)

Endpoints

Primary endpoints: Safety endpoints including, vital signs, ECG parameters, clinical laboratory parameters

Secondary endpoints: Efficacy endpoints including change from baseline/over time in relevant neurological endpoints for each patient group (NPI, MMSE, ADHD-RS, ADOS, BPDCL)

Key inclusion criteria

Significant or persistent agitation or aggression that was disruptive to patient’s daily living or put the patient at risk of harm for at least three days per week for at least four weeks prior to screening visit.

Stable pharmacological treatment as per SmPC of AD, LBD, ADHD, BPD or ASD for at least four months (with the same dose for at least two months) prior to screening – including anti-inflammatories.

Sites

Hospital Vall d’Hebrón, Barcelona

Timelines

Study start: October 2018, last patient out: Q119

Source: EU Clinical Trials Register, Oryzon. Notes: TEAE: Treatment Emergent Adverse Events; NPI: Neuropsychiatric Inventory Questionnaire; MMSE: Mini-Mental State Examination; ADHD-RS: Attention-Deficit/Hyperactivity Disorder Rating Scale; ADOS: Autism Diagnostic Observation Schedule; BPDCL: Borderline Personality Disease Checklist.

Data from vafidemstat in AD and MS also expected this year

Two other Phase IIa trials with ORY-2001 are underway:

A randomised, double-blind, placebo-controlled, 36-week Phase IIa SATEEN study (n=24) will evaluate ORY-2001 in patients with relapsing-remitting MS and secondary progressive MS.

A second randomised, double-blind, placebo-controlled, 24-week Phase IIa ETHERAL trial (n=90) with ORY-2001 in mild to moderate AD started enrolling patients in May 2018.

The preliminary data readouts from both studies are expected in Q319 and Q419 (Exhibit 2).

Iadademstat: First preliminary data readouts from ALICE and CLEPSIDRA trials likely in Q219

Two Phase IIa studies with iadademstat, a specific LSD1 inhibitor, are ongoing. The Phase IIa ALICE study will recruit elderly AML patients (n=36) who will receive ORY-1001 in combination with standard of care, azacitidine. The other Phase IIa CLEPSIDRA trial will recruit relapsed SCLC patients (n=36) who will receive iadademstat in combination with platinum-etoposide chemotherapy. Interim results from both studies are expected in 2019 with the first significant presentations likely to be first data from the CLESPIDRA study at the ASCO conference (31 May - 4 June 2019 and) the ALICE study at the EHA conference (13 June - 16 June 2019).

One of the main goals of these trials is to understand how iadademstat works in combination with various other drugs. To this end, an article published in Cell by a third-party research team at Harvard Medical School described the findings that inhibiting LSD1 could lead to the activation of immune response and overcome resistance to anti-PD-1 therapy. We reviewed key data on iadademstat and the article in Cell in our last outlook report.

Most recent relevant third party publication (Augert et al) provided more insights about the mechanism of action of iadademstat in SCLC. While the drug was shown to be effective in SCLC models before, the details of actual mechanism of action were still missing. The team of researchers from Fred Hutchinson Cancer Research Center and the Department of Genome Sciences, University of Washington (Seattle, WA, US) found that selective inhibition of LSD1 with iadademstat activated the NOTCH pathway, resulting in the suppression of the transcription factor ASCL1. This in turn suppressed SCLC development. In vivo patient-derived xenograft (PDX) models showed that there was a correlation between extent of NOTCH pathway activation and suppression of the tumour growth. Furthermore, complete and durable tumor regression occurred using iadademstat in a chemoresistant PDX model.

The NOTCH signalling pathway is a highly conserved cell system present in most multicellular organisms. The transcription factor ASCL1 appears to play an important role in SCLC development, but it is not suitable as a target for classical drug development, ie not “druggable”, while iadademstat appears to achieve that through activation of NOTCH and now has a demonstrated proof-of-concept in in vivo models.

Exhibit 4: Iadademstat near-term catalysts

Source: Oryzon

Valuation

Our valuation is slightly higher at €364m or €9.3 per share (from €342m or €8.7/share per share) due to rolling our model forward. As Oryzon is on track to develop its assets in all the indications we include in our valuation, we leave our assumptions unchanged. Since cash reaches well into H220, the existing cash is sufficient to deliver meaningful data from all ongoing trials.

Exhibit 5: Oryzon rNPV valuation

Product

Indication

Launch

Peak sales
(US$m)

Value
(€m)

Probability of success (%)

rNPV
(€m)

NPV/share
(€/share)

Iadademstat (ORY-1001)

AML

2023

927

284.1

15%

56.3

1.4

Iadademstat (ORY-1001)

SCLC

2026

571

137.6

8%

25.2

0.6

Vafidemstat (ORY-2001)

AD

2026

4,510

1,018.3

15%

160.5

4.1

Vafidemstat (ORY-2001)

MS

2027

1,940

446.6

20%

105.8

2.7

Net cash (end-2018)

16.2

100%

16.2

0.4

Valuation

 

 

1,902.8

364.0

9.3

Source: Edison Investment Research

Exhibit 6: Financial summary

€'000s

 

2016

2017

2018

2019e

2020e

December

Local GAAP

Local GAAP

Local GAAP

Local GAAP

Local GAAP

PROFIT & LOSS

Revenue

 

 

5,009

4,317

6,781

6,119

6,137

Cost of Sales

0

0

0

0

0

Gross Profit

5,009

4,317

6,781

6,119

6,137

Research and development

(5,210)

(5,306)

(7,412)

(9,454)

(9,560)

EBITDA

 

 

(3,721)

(3,498)

(2,766)

(6,046)

(6,175)

Operating Profit (before amort. and except.)

(3,879)

(3,660)

(2,905)

(6,186)

(6,314)

Intangible Amortisation

(695)

(664)

(7)

(8)

(9)

Exceptionals

(4)

0

(4)

0

0

Other

0

0

0

0

0

Operating Profit

(4,578)

(4,324)

(2,916)

(6,194)

(6,324)

Exceptionals

(58)

0

0

0

0

Net Interest

(844)

(928)

(796)

(586)

(471)

Profit Before Tax (norm)

 

 

(4,724)

(4,588)

(3,701)

(6,771)

(6,786)

Profit Before Tax (reported)

 

 

(5,480)

(5,252)

(3,712)

(6,780)

(6,795)

Tax

32

55

2,535

0

0

Profit After Tax (norm)

(4,692)

(4,533)

(1,166)

(6,771)

(6,786)

Profit After Tax (reported)

(5,448)

(5,197)

(1,177)

(6,780)

(6,795)

Average Number of Shares Outstanding (m)

27.6

31.7

34.6

39.1

39.1

EPS - normalised (€)

 

 

(0.17)

(0.14)

(0.03)

(0.17)

(0.17)

EPS - reported (€)

 

 

(0.20)

(0.16)

(0.03)

(0.17)

(0.17)

Dividend per share (€)

0.0

0.0

0.0

0.0

0.0

Gross Margin (%)

100.0

100.0

100.0

100.0

100.0

EBITDA Margin (%)

N/A

N/A

N/A

N/A

N/A

Operating Margin (before GW and except.) (%)

N/A

N/A

N/A

N/A

N/A

BALANCE SHEET

Fixed Assets

 

 

21,269

24,914

31,786

37,758

43,807

Intangible Assets

18,810

22,458

29,330

35,441

41,569

Tangible Assets

696

638

665

526

447

Investments

1,763

1,818

1,791

1,791

1,791

Current Assets

 

 

28,475

36,130

35,664

16,488

3,856

Stocks

8

7

135

71

103

Debtors

978

857

971

914

943

Cash

22,028

34,950

34,320

15,264

2,572

Other

5,461

316

239

239

239

Current Liabilities

 

 

(7,597)

(8,696)

(10,441)

(4,017)

(4,229)

Creditors

(2,119)

(1,343)

(2,192)

(1,767)

(1,979)

Short term borrowings

(5,477)

(7,354)

(8,249)

(2,249)

(2,249)

Long Term Liabilities

 

 

(19,419)

(17,915)

(11,884)

(11,884)

(11,884)

Long term borrowings

(17,723)

(16,041)

(9,977)

(9,977)

(9,977)

Other long term liabilities

(1,696)

(1,874)

(1,907)

(1,907)

(1,907)

Net Assets

 

 

22,729

34,432

45,125

38,345

31,550

CASH FLOW

Operating Cash Flow

 

 

(4,536)

(4,281)

(2,799)

(6,936)

(6,495)

Net Interest

(471)

(426)

2,133

(586)

(471)

Tax

0

0

0

0

0

Capex

(28)

(105)

(170)

0

0

Acquisitions/disposals

0

0

0

0

0

Financing

287

16,887

11,949

0

0

Other*

(6,819)

653

(6,576)

(5,534)

(5,726)

Dividends

0

0

0

0

0

Net Cash Flow

(11,567)

12,728

4,538

(13,055)

(12,692)

Opening net debt/(cash)

 

 

(10,395)

1,172

(11,555)

(16,093)

(3,038)

HP finance leases initiated

0

0

0

0

0

Other

0

0

0

0

0

Closing net debt/(cash)

 

 

1,172

(11,555)

(16,093)

(3,038)

9,655

Source: Edison Investment Research, Oryzon Genomics accounts. Note: Oryzon reports in Spanish GAAP. *Includes cash outflows related to development costs that were capitalised.

General disclaimer and copyright

This report has been commissioned by Oryzon Genomics and prepared and issued by Edison, in consideration of a fee payable by Oryzon Genomics. Edison Investment Research standard fees are £49,500 pa for the production and broad dissemination of a detailed note (Outlook) following by regular (typically quarterly) update notes. Fees are paid upfront in cash without recourse. Edison may seek additional fees for the provision of roadshows and related IR services for the client but does not get remunerated for any investment banking services. We never take payment in stock, options or warrants for any of our services.

Accuracy of content: All information used in the publication of this report has been compiled from publicly available sources that are believed to be reliable, however we do not guarantee the accuracy or completeness of this report and have not sought for this information to be independently verified. Opinions contained in this report represent those of the Edison analyst at the time of publication. Forward-looking information or statements in this report contain information that is based on assumptions, forecasts of future results, estimates of amounts not yet determinable, and therefore involve known and unknown risks, uncertainties and other factors which may cause the actual results, performance or achievements of their subject matter to be materially different from current expectations.

Exclusion of Liability: To the fullest extent allowed by law, Edison shall not be liable for any direct, indirect or consequential losses, loss of profits, damages, costs or expenses incurred or suffered by you arising out or in connection with the access to, use of or reliance on any information contained on this note.

No personalised advice: The information that we provide should not be construed in any manner whatsoever as, personalised advice. Also, the information provided by us should not be construed by any subscriber or prospective subscriber as Edison’s solicitation to effect, or attempt to effect, any transaction in a security. The securities described in the report may not be eligible for sale in all jurisdictions or to certain categories of investors.

Investment in securities mentioned: Edison has a restrictive policy relating to personal dealing and conflicts of interest. Edison Group does not conduct any investment business and, accordingly, does not itself hold any positions in the securities mentioned in this report. However, the respective directors, officers, employees and contractors of Edison may have a position in any or related securities mentioned in this report, subject to Edison's policies on personal dealing and conflicts of interest.

Copyright: Copyright 2019 Edison Investment Research Limited (Edison). All rights reserved FTSE International Limited (“FTSE”) © FTSE 2019. “FTSE®” is a trade mark of the London Stock Exchange Group companies and is used by FTSE International Limited under license. All rights in the FTSE indices and/or FTSE ratings vest in FTSE and/or its licensors. Neither FTSE nor its licensors accept any liability for any errors or omissions in the FTSE indices and/or FTSE ratings or underlying data. No further distribution of FTSE Data is permitted without FTSE’s express written consent.

Australia

Edison Investment Research Pty Ltd (Edison AU) is the Australian subsidiary of Edison. Edison AU is a Corporate Authorised Representative (1252501) of Myonlineadvisers Pty Ltd who holds an Australian Financial Services Licence (Number: 427484). This research is issued in Australia by Edison AU and any access to it, is intended only for "wholesale clients" within the meaning of the Corporations Act 2001 of Australia. Any advice given by Edison AU is general advice only and does not take into account your personal circumstances, needs or objectives. You should, before acting on this advice, consider the appropriateness of the advice, having regard to your objectives, financial situation and needs. If our advice relates to the acquisition, or possible acquisition, of a particular financial product you should read any relevant Product Disclosure Statement or like instrument.

New Zealand

The research in this document is intended for New Zealand resident professional financial advisers or brokers (for use in their roles as financial advisers or brokers) and habitual investors who are “wholesale clients” for the purpose of the Financial Advisers Act 2008 (FAA) (as described in sections 5(c) (1)(a), (b) and (c) of the FAA). This is not a solicitation or inducement to buy, sell, subscribe, or underwrite any securities mentioned or in the topic of this document. For the purpose of the FAA, the content of this report is of a general nature, is intended as a source of general information only and is not intended to constitute a recommendation or opinion in relation to acquiring or disposing (including refraining from acquiring or disposing) of securities. The distribution of this document is not a “personalised service” and, to the extent that it contains any financial advice, is intended only as a “class service” provided by Edison within the meaning of the FAA (i.e. without taking into account the particular financial situation or goals of any person). As such, it should not be relied upon in making an investment decision.

United Kingdom

Neither this document and associated email (together, the "Communication") constitutes or form part of any offer for sale or subscription of, or solicitation of any offer to buy or subscribe for, any securities, nor shall it or any part of it form the basis of, or be relied on in connection with, any contract or commitment whatsoever. Any decision to purchase shares in the Company in the proposed placing should be made solely on the basis of the information to be contained in the admission document to be published in connection therewith.

This Communication is being distributed in the United Kingdom and is directed only at (i) persons having professional experience in matters relating to investments, i.e. investment professionals within the meaning of Article 19(5) of the Financial Services and Markets Act 2000 (Financial Promotion) Order 2005, as amended (the "FPO") (ii) high net-worth companies, unincorporated associations or other bodies within the meaning of Article 49 of the FPO and (iii) persons to whom it is otherwise lawful to distribute it. The investment or investment activity to which this document relates is available only to such persons. It is not intended that this document be distributed or passed on, directly or indirectly, to any other class of persons and in any event and under no circumstances should persons of any other description rely on or act upon the contents of this document (nor will such persons be able to purchase shares in the placing).

This Communication is being supplied to you solely for your information and may not be reproduced by, further distributed to or published in whole or in part by, any other person.

United States

The Investment Research is a publication distributed in the United States by Edison Investment Research, Inc. Edison Investment Research, Inc. is registered as an investment adviser with the Securities and Exchange Commission. Edison relies upon the "publishers' exclusion" from the definition of investment adviser under Section 202(a) (11) of the Investment Advisers Act of 1940 and corresponding state securities laws. This report is a bona fide publication of general and regular circulation offering impersonal investment-related advice, not tailored to a specific investment portfolio or the needs of current and/or prospective subscribers. As such, Edison does not offer or provide personal advice and the research provided is for informational purposes only. No mention of a particular security in this report constitutes a recommendation to buy, sell or hold that or any security, or that any particular security, portfolio of securities, transaction or investment strategy is suitable for any specific person.

Frankfurt +49 (0)69 78 8076 960

Schumannstrasse 34b

60325 Frankfurt

Germany

London +44 (0)20 3077 5700

280 High Holborn

London, WC1V 7EE

United Kingdom

New York +1 646 653 7026

1,185 Avenue of the Americas

3rd Floor, New York, NY 10036

United States of America

Sydney +61 (0)2 8249 8342

Level 4, Office 1205

95 Pitt Street, Sydney

NSW 2000, Australia

Frankfurt +49 (0)69 78 8076 960

Schumannstrasse 34b

60325 Frankfurt

Germany

London +44 (0)20 3077 5700

280 High Holborn

London, WC1V 7EE

United Kingdom

New York +1 646 653 7026

1,185 Avenue of the Americas

3rd Floor, New York, NY 10036

United States of America

Sydney +61 (0)2 8249 8342

Level 4, Office 1205

95 Pitt Street, Sydney

NSW 2000, Australia

More on Oryzon Genomics

View All

Latest from the Healthcare sector

View All Healthcare content

Research: Healthcare

Acacia Pharma — Ready for BARHEMSYS launch in H119

Acacia Pharma has now established its initial US sales and marketing infrastructure, ahead of the potential launch of lead asset BARHEMSYS. This is the first step in its strategy to bring antiemetic drugs to the hospital setting for unmet needs in PONV and CINV. The FDA has accepted Acacia’s revised New Drug Application (NDA) for BARHEMSYS and has now set a Prescription Drug User Fee Act (PDUFA) date of 5 May. We continue to expect launch of BARHEMSYS in H119. We value Acacia at €635m (or €11.9/share) vs €602m (or €11.3/share) previously.

Continue Reading

Subscribe to Edison

Get access to the very latest content matched to your personal investment style.

Sign up for free