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.€120.8m
Last close€8.65
High / Low (52 weeks)€12.3 / €7.5
Stock market listingEU
Forecast net cash (€m)3.8
Forecast gearing ratio (%)N/A
TeamHealthcare
SectorPharmaceutical & healthcare

Price performance

%1m3m12m
Actual4.93.1(13.5)
Relative *1.8(3)(25.2)

* % Relative to local index

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Company news

Investment summary

Kiadis Pharma is developing T cell-based therapies to address the issues associated with haematopoietic stem cell transplantation (HSCT). The company is leveraging 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 is aiming for accelerated filing of ATIR101 with the European Medicines Agency (EMA) in Q117. A Phase III trial has started in February 2017. ATIR201 has started a Phase I/II trial with data expected in H217. Cash at end June 2016 was €23.7m, sufficient to fund operations until early 2018.

Last updated on 02/03/2017

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 09/02/2017

Latest video

Executive Interview - Kiadis

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 American Society of Hematology 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 02/03/2017

Key management

Manfred Ruediger, CEO
Robbert van Heekeren, CFO

Company address

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