Kiadis Pharma (KDS)

Business description

Kiadis Pharma is a biotech company focused on cell-based immunotherapies to overcome complications associated with stem cell transplants in blood diseases. ATIR101 for leukaemia is in Phase II and will file for EU approval in Q117. ATIR201 (thalassemia) started a Phase I/II in December 2016.

Stock data

Market cap.€87.1m
Last close€5.92
High / Low (52 weeks)€11.8 / €5.2
Stock market listingEU
Forecast net cash (€m)3.8
Forecast gearing ratio (%)N/A
TeamHealthcare
SectorPharmaceutical & healthcare

Price performance

%1m3m12m
Actual5.6(28.2)(48.9)
Relative *4.6(26.8)(56.2)

* % Relative to local index

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Company news

Research delivers insight into the hematopoietic stem cell transplantation

Tue, 07 Feb 2017 10:52:30 GMT

Kiadis Pharma obtains up to €15 million debt financing from Kreos Capital

Thu, 17 Aug 2017 10:41:15 GMT

Kiadis Pharma NV: Planned Management Team Changes

Thu, 08 Dec 2016 06:00:35 GMT

Kiadis Pharma proposes former Actelion COO Otto Schwarz as new Supervisory ...

Wed, 26 Jul 2017 04:52:30 GMT

Kiadis Pharma issues clinical and regulatory progress update on ATIR101™ and ...

Mon, 06 Feb 2017 06:00:00 GMT

Y/E Dec Revenue (€m) EBITDA (€m) PBT (€m) EPS (c) P/E (x) P/CF (x)
2014A 0.0 (6.0) (7.2) (74.62) N/A N/A
2015A 0.0 (15.9) (17.4) (136.50) N/A N/A
2016E 0.0 (8.6) (10.0) (71.58) N/A N/A
2017E 0.0 (11.9) (13.5) (96.42) N/A N/A

Last updated on 14/07/2017

Investment summary

Kiadis Pharma is developing T cell-based therapies to address the issues associated with haematopoietic stem cell transplantation (HSCT). The company uses its Theralux technology to develop ATIR101 and ATIR201 as adjunct therapies to HSCT in leukaemia and thalassemia, respectively. On the back of Phase II data, Kiadis filed a Marketing Authorisation Application (MAA) of ATIR101 with the European Medicines Agency (EMA) in April 2017. A Phase III trial started in February 2017. ATIR201 is undergoing a Phase I/II trial with data expected in H217. Cash at end 2016 was €14.6m. Kiadis raised €5m in a private placement in June 2017.

Last updated on 03/08/2017

Industry outlook

Kiadis's Theralux platform allows the infusion of lymphocytes from a partially matching (haploidentical) family member to the donor as it eliminates cells that could react against the host’s immune cells and cause complications such as Graft vs Host Diasease (GVHD). Positive one year data (Event-Free Survival and Overall Survival) from Phase II clinical trial with ATIR101 was presented at the ASH 58th Annual Meeting in San Diego, USA. Overall survival was 61% for the ATIR101 arm vs 20% of a historic control group receiving HSCT only. GFRS was 57% for HSCT+ATIR101 vs 20% for the control group.

Last updated on 03/08/2017

Key management

Arthur Lahr, CEO
Robbert van Heekeren, CFO

Company address

Entrada 231-234
1114 AA, Amsterdam, The Netherlands
Netherlands
+31 (0)20 314 02 50
View website